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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
10-Q
☒
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For
the quarterly period ended September 30, 2024
☐
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
333-275062
Commission
file number
Impact
BioMedical, INC. |
(Exact
name of registrant as specified in its charter) |
Nevada |
|
85-3926944 |
(State
or other Jurisdiction of |
|
(IRS
Employer |
incorporation-
or Organization) |
|
Identification
No.) |
1400 Broadfield Blvd., Suite 130,
Houston,
Tx, 77084
(Address
of principal executive offices)
(281)
415-6576
(Registrant’s
telephone number, including area code)
Indicate
by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange
Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2)
has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐
Indicate
by check mark whether the registrant has submitted electronically every Interactive Date File required to be submitted pursuant to Rule
405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant
was required to submit such files) Yes ☒ No ☐
Indicate
by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting
company, or an emerging growth company. See definitions of “large accelerated filer”, “accelerated filer”, “smaller
reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
Large
accelerated filer ☐ |
Accelerated
filer ☐ |
Non-accelerated
filer ☒ |
Smaller
reporting company ☒ |
|
|
|
|
Emerging
growth company ☒ |
|
|
|
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
Indicate
by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act) Yes ☐ No ☒
Securities
registered pursuant to Section 12(b) of the Act:
Title
of each class |
|
Ticker
symbol(s) |
|
Name
of each exchange on which registered |
Common
Stock, $0.001 par value per share |
|
N/A |
|
N/A |
As
of October 25, 2024 there were 11,503,955 shares of the registrant’s common stock, $0.001 par value, outstanding.
IMPACT
BIOMEDICAL, INC.
FORM
10-Q
TABLE
OF CONTENTS
Impact
BioMedical Inc and Subsidiaries
Condensed
Consolidated Balance Sheets
| |
September 30, 2024 (unaudited) | | |
December 31, 2023 | |
ASSETS | |
| | | |
| | |
Current assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 2,668,000 | | |
$ | 1,000 | |
Accounts receivable, net | |
| - | | |
| 128,000 | |
Current portion of notes receivable | |
| 142,000 | | |
| 203,000 | |
Prepaid expenses and other current assets | |
| 365,000 | | |
| - | |
Total current assets | |
| 3,175,000 | | |
| 332,000 | |
| |
| | | |
| | |
Property, plant and equipment, net | |
| 282,000 | | |
| 287,000 | |
Notes receivable | |
| 59,000 | | |
| - | |
Goodwill | |
| 25,093,000 | | |
| 25,093,000 | |
Other intangible assets, net | |
| 18,086,000 | | |
| 18,921,000 | |
Total assets | |
$ | 46,695,000 | | |
$ | 44,633,000 | |
| |
| | | |
| | |
LIABILITIES AND STOCKHOLDERS’ EQUITY | |
| | | |
| | |
| |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable | |
$ | 1,001,000 | | |
$ | 832,000 | |
Accrued expenses and deferred revenue | |
| 102,000 | | |
| 230,000 | |
Current portion note payable, related party | |
| 35,000 | | |
| 12,074,000 | |
Total current liabilities | |
| 1,138,000 | | |
| 13,136,000 | |
| |
| | | |
| | |
Long-term portion note payable, related party | |
| 7,971,000 | | |
| - | |
Deferred tax liability, net | |
| 3,235,000 | | |
| 3,235,000 | |
Total liabilities | |
| 12,344,000 | | |
| 16,371,000 | |
| |
| | | |
| | |
Commitments and contingencies (Note 11) | |
| - | | |
| - | |
| |
| | | |
| | |
Stockholders’ equity | |
| | | |
| | |
Preferred stock, $.001 par value; 100,000,000 shares authorized, 60,496,041 shares issued and outstanding (60,496,041 on December 31, 2023); Liquidation value $0.001 per share, $60,000 aggregate. $60,000 on December 31, 2023). | |
| 60,000 | | |
| 60,000 | |
Common stock, $.001 par value; 4,000,000,000 shares authorized, 11,503,955 shares issued and outstanding (10,000,000 on December 31, 2023) | |
| 11,000 | | |
| 10,000 | |
Additional paid-in capital | |
| 41,838,000 | | |
| 38,113,000 | |
Accumulated deficit | |
| (10,561,000 | ) | |
| (12,961,000 | ) |
Total stockholders’ equity of the Company | |
| 31,348,000 | | |
| 25,222,000 | |
Non-controlling interest in subsidiaries | |
| 3,003,000 | | |
| 3,040,000 | |
Total stockholders’ equity | |
| 34,351,000 | | |
| 28,262,000 | |
| |
| | | |
| | |
Total liabilities and stockholders’ equity | |
$ | 46,695,000 | | |
$ | 44,633,000 | |
See
accompanying notes to the consolidated financial statements.
Impact
BioMedical Inc and Subsidiaries
Condensed
Consolidated Statements of Operations
(unaudited)
| |
| | |
| | |
| | |
| |
| |
For the Three Months Ended September 30, | | |
For the Nine Months Ended September 30, | |
| |
2024 | | |
2023 | | |
2024 | | |
2023 | |
Costs and expenses: | |
| | | |
| | | |
| | | |
| | |
Sales, general and administrative compensation | |
| 132,000 | | |
| 101,000 | | |
| 424,000 | | |
| 182,000 | |
Sales and marketing | |
| 461,000 | | |
| 17,000 | | |
| 487,000 | | |
| 44,000 | |
Professional Fees | |
| 122,000 | | |
| 317,000 | | |
| 313,000 | | |
| 750,000 | |
Research and development | |
| 82,000 | | |
| 357,000 | | |
| 386,000 | | |
| 1,055,000 | |
Depreciation and Amortization | |
| 281,000 | | |
| 280,000 | | |
| 840,000 | | |
| 840,000 | |
Rent and utilities | |
| 4,000 | | |
| - | | |
| 14,000 | | |
| - | |
Other operating expenses | |
| 45,000 | | |
| 6,000 | | |
| 58,000 | | |
| 18,000 | |
Total costs and expenses | |
| 1,127,000 | | |
| 1,078,000 | | |
| 2,522,000 | | |
| 2,889,000 | |
| |
| | | |
| | | |
| | | |
| | |
Operating loss | |
| (1,127,000 | ) | |
| (1,078,000 | ) | |
| (2,522,000 | ) | |
| (2,889,000 | ) |
| |
| | | |
| | | |
| | | |
| | |
Other income (expense): | |
| | | |
| | | |
| | | |
| | |
Interest income | |
| 3,000 | | |
| 3,000 | | |
| 10,000 | | |
| 10,000 | |
Change in fair value of embedded derivative | |
| 5,670,000 | | |
| - | | |
| 5,670,000 | | |
| - | |
Other income (expense) | |
| - | | |
| - | | |
| - | | |
| 52,000 | |
Interest expense | |
| (305,000 | ) | |
| (102,000 | ) | |
| (795,000 | ) | |
| (319,000 | ) |
| |
| | | |
| | | |
| | | |
| | |
| |
| | | |
| | | |
| | | |
| | |
Income tax benefit | |
| - | | |
| - | | |
| - | | |
| - | |
Net income (loss) | |
$ | 4,241,000 | | |
$ | (1,177,000 | ) | |
$ | 2,363,000 | | |
$ | (3,146,000 | ) |
| |
| | | |
| | | |
| | | |
| | |
Loss from operations attributed to noncontrolling interest | |
| 6,000 | | |
| 15,000 | | |
| 37,000 | | |
| 45,000 | |
| |
| | | |
| | | |
| | | |
| | |
Income (loss) attributable to common stockholders | |
$ | 4,247,000 | | |
$ | (1,162,000 | ) | |
$ | 2,400,000 | | |
$ | (3,101,000 | ) |
| |
| | | |
| | | |
| | | |
| | |
Income (loss) per common share: | |
| | | |
| | | |
| | | |
| | |
Basic | |
$ | 0.37 | | |
$ | (0.02 | ) | |
$ | 0.23 | | |
$ | (0.04 | ) |
Diluted | |
$ | 0.06 | | |
$ | (0.02 | ) | |
$ | 0.03 | | |
$ | (0.04 | ) |
| |
| | | |
| | | |
| | | |
| | |
Shares used in computing loss per common share: | |
| | | |
| | | |
| | | |
| | |
Basic | |
| 11,503,955 | | |
| 70,496,041 | | |
| 10,506,394 | | |
| 70,496,041 | |
Diluted | |
| 71,999,996 | | |
| 70,496,041 | | |
| 71,002,435 | | |
| 70,496,041 | |
See
accompanying notes to the consolidated financial statements.
Impact
BioMedical Inc and Subsidiaries
Condensed
Consolidated Statements of Stockholder’s Equity
(unaudited)
| |
| | |
| | |
| | |
| | |
| | |
| | |
| | |
| | |
| |
| |
Common Stock | | |
Preferred Stock | | |
Additional
Paid-in | | |
Accumulated | | |
Total Impact
| | |
Non- controlling
Interest in | | |
| |
| |
Shares | | |
Amount | | |
Shares | | |
Amount | | |
Capital | | |
Deficit | | |
Equity | | |
Subsidiary | | |
Total | |
| |
| | |
| | |
| | |
| | |
| | |
| | |
| | |
| | |
| |
Balance, December 31, 2022 | |
| 70,496,041 | | |
$ | 70,000 | | |
| - | | |
$ | - | | |
$ | 38,113,000 | | |
$ | (8,567,000 | ) | |
$ | 29,616,000 | | |
| 3,111,000 | | |
$ | 32,727,000 | |
| |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Net loss | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| (3,101,000 | ) | |
| (3,101,000 | ) | |
| (45,000 | ) | |
| (3,146,000 | ) |
Balance, September 30, 2023 | |
| 70,496,041 | | |
$ | 70,000 | | |
| - | | |
$ | - | | |
$ | 38,113,000 | | |
$ | (11,668,000 | ) | |
$ | 26,515,000 | | |
$ | 3,066,000 | | |
$ | 29,581,000 | |
| |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Balance, December 31, 2023 | |
| 10,000,000 | | |
$ | 10,000 | | |
| 60,496,041 | | |
$ | 60,000 | | |
$ | 38,113,000 | | |
$ | (12,961,000 | ) | |
$ | 25,222,000 | | |
$ | 3,040,000 | | |
$ | 28,262,000 | |
Balance | |
| 10,000,000 | | |
$ | 10,000 | | |
| 60,496,041 | | |
$ | 60,000 | | |
$ | 38,113,000 | | |
$ | (12,961,000 | ) | |
$ | 25,222,000 | | |
$ | 3,040,000 | | |
$ | 28,262,000 | |
| |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Issuance of common stock, net of expenses | |
| 1,500,000 | | |
| 1,000 | | |
| - | | |
| - | | |
| 3,725,000 | | |
| - | | |
| 3,726,000 | | |
| - | | |
| 3,726,000 | |
Fractional shares as a result of reverse stock split | |
| 3,955 | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | |
Net income (loss) | |
| - | | |
| - | | |
| - | | |
| - | | |
| - | | |
| 2,400,000 | | |
| 2,400,000 | | |
| (37,000 | ) | |
| 2,363,000 | |
Balance, September 30, 2024 | |
| 11,503,955 | | |
$ | 11,000 | | |
| 60,496,041 | | |
$ | 60,000 | | |
$ | 41,838,000 | | |
$ | (10,561,000 | ) | |
$ | 31,348,000 | | |
$ | 3,003,000 | | |
$ | 34,351,000 | |
Balance | |
| 11,503,955 | | |
$ | 11,000 | | |
| 60,496,041 | | |
$ | 60,000 | | |
$ | 41,838,000 | | |
$ | (10,561,000 | ) | |
$ | 31,348,000 | | |
$ | 3,003,000 | | |
$ | 34,351,000 | |
See
accompanying notes to the consolidated financial statements.
Impact
BioMedical Inc and Subsidiaries
Condensed
Consolidated Statements of Cash Flows
For
the Nine Months Ended September 30,
(unaudited)
| |
2024 | | |
2023 | |
Cash flows from operating activities: | |
| | | |
| | |
Income (loss) from operations | |
$ | 2,363,000 | | |
$ | (3,146,000 | ) |
Adjustments to reconcile loss from continuing operations to net cash used by operating activities: | |
| | | |
| | |
Depreciation and amortization | |
| 840,000 | | |
| 840,000 | |
Change in fair value of embedded derivative | |
| (5,670,000 | ) | |
| - | |
Decrease (increase) in assets: | |
| | | |
| | |
Accounts receivable | |
| 128,000 | | |
| - | |
Prepaid expenses and other current assets | |
| (365,000 | ) | |
| 8,000 | |
Increase (decrease) in liabilities: | |
| | | |
| | |
Accounts payable | |
| 169,000 | | |
| (63,000 | ) |
Accrued expenses | |
| (128,000 | ) | |
| (57,000 | ) |
Net cash used by operating activities | |
| (2,663,000 | ) | |
| (2,418,000 | ) |
| |
| | | |
| | |
Cash flows from investing activities: | |
| | | |
| | |
Purchase of property, plant and equipment | |
| - | | |
| (18,000 | ) |
Payments received on notes receivable | |
| 2,000 | | |
| 2,000 | |
Net cash provided (used) by investing activities | |
| 2,000 | | |
| (16,000 | ) |
| |
| | | |
| | |
Cash flows from financing activities: | |
| | | |
| | |
Borrowings from revolving lines of credit, net | |
| 1,602,000 | | |
| 2,633,000 | |
Issuances of common stock, net of issuance costs | |
| 3,726,000 | | |
| - | |
Net cash provided by financing activities | |
| 5,328,000 | | |
| 2,633,000 | |
| |
| | | |
| | |
Net increase in cash | |
| 2,667,000 | | |
| 199,000 | |
Cash and cash equivalents at beginning of period | |
| 1,000 | | |
| 2,000 | |
Cash and cash equivalents at end of period | |
$ | 2,668,000 | | |
$ | 201,000 | |
See
accompanying notes to the consolidated financial statements.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Note
1. Nature of Operations and Basis of Presentation
Nature
of Operations
Impact
BioMedical, Inc., incorporated in the State of Nevada
on October
16, 2018 (the “Company”, “Impact
BioMedical”, “We”, “IBO”), discovers, confirms, and patents unique science and technologies which
can be developed into new offerings in human healthcare and wellness in collaboration with external partners through licensing, co-development,
joint ventures, and other relationships. By leveraging technology and new science with strategic partnerships, we pursue advances
in biopharmaceuticals and over the counter direct to consumer wellness offerings. In addition to existing efforts, we continually
search for and evaluate other potential new offerings to add to our portfolio. Our business model includes partnering and potentially
direct sales for commercialization and distribution. Potential licensors and development partners include pharmaceutical, consumer goods
and services companies and others, who would commercialize IBO technologies in exchange for milestone, and royalty licensing payments.
Impact
has several unique and proprietary technologies that are in continuing development:
Linebacker™
Linebacker is a platform of
small molecule electrophilically enhanced polyphenol compounds with potential application in oncology (solid tumors), inflammatory disorders,
and neurology. Polyphenols are substances found in many nuts, vegetables, and berries. Linebacker compounds are modified Myricetin,
which is a common plant-derived flavonoid. Myricetin exhibits a wide range of activities that include strong antioxidants and anti-inflammatory
activities (source: NIH). Linebacker can potentially be developed as monotherapy or co-therapy to down-regulate PIM (proviral integration
site for Moloney murine leukemia virus) kinase which plays a key role as an oncogene in various cancers (e.g., colon, lung, prostate,
breast). Additional potential applications include inflammatory disorders and neurology. Linebacker-1 and Linebacker-2 compounds
have been licensed to ProPhase Laboratories (NASDAQ: PRPH) for development and potential commercialization worldwide, from which Impact
Biomedical could receive future milestone and royalty payments. Composition and method patents are issued to the company for Linebacker
in the U.S. and other countries.
Laetose™
Laetose technology is derived
from a unique combination of multiple sugars independently with myo-inositol, which demonstrates compelling potential in 1) reducing glycemic
index and caloric intake in foods, 2) application as a therapeutic which inhibits tumor necrosis factor alpha (TNF-α), a cytokine
associated with inflammatory chronic diseases, and 3) a method of reducing or limiting the occurrence of diabetes. The sugar can
be one or a combination of sugars: sucrose, fructose, isoglucose, and galactose. Laetose has a unique composition patent allowed in the
United States and patents are pending in other countries worldwide. IBO is actively seeking potential partners for further development
and commercialization of Laetose as a consumer packaged or biopharmaceutical offering worldwide.
Functional
Fragrance Formulation (“3F”)
3F is a suite of organic “functional
fragrances” containing specialized botanical ingredients (e.g., terpenes) with potential application as an antimicrobial, or as
an additive in insect repellents, detergents, lotions, shampoo, fabrics, and other substances to increase effectiveness. IBO has
partnered with the Chemia Corporation (St. Louis, MO) to pursue development of the 3F technology. Chemia is a leading developer and manufacturer
of fragrances and flavors. Composition patents have issued in the U.S. and are pending in other countries. In addition to Chemia,
IBO is actively seeking potential partners for the further development and commercialization of 3F worldwide, given the broad application
of this technology.
Equivir™/Equivir
G
Equivir technology is a novel
blend of FDA Generally Recognized as Safe (GRAS) eligible polyphenols (e.g., Myricetin, Hesperetin, Piperine) which have demonstrated
antiviral effects with additional potential applications such as health supplements or medication. Polyphenols are substances found in
many nuts, vegetables, and berries. Myricetin is a member of the flavonoid class of polyphenolic compounds with antioxidant properties.
Hesperitin is a flavanone and Piperine is an alkaloid, commonly found in black pepper. Equivir/Equivir G is licensed to ProPhase
Laboratories for development and commercialization worldwide. ProPhase Lab’s initial focus is for potential use as an over-the-counter
health supplement offering for upper respiratory wellness. Additional applications could be pursued in the future. Method and composition
patents are issued in the U.S. and other countries.
Emerging
Technology
IBO
continually evaluates additional technologies that are in various phases of development which can be advanced to patent filings and allowances.
These include, and are not limited to biopharmaceuticals, indoor air quality products, preservatives, bioplastics, personalized medicine
(e.g., genomics, diagnostics), nanotechnology, cannabis products and technology, pain management, and others. These activities
include discussions with inventors, scientists, universities, research foundations, and other parties, which, subject to completion
of diligence, and approval of the respective management, could potentially expand the offerings of IBO.
As
of the date of this report, we have not generated significant revenues from operations. We cannot guarantee we will be successful in
our business operations. Our business is subject to risks inherent in the establishment of a new business enterprise, including possible
delays in our research, testing and marketing efforts or wider economic downturns.
Note
2. Summary of Significant Accounting and Reporting Policies
Basis
of Presentation and Principles of Consolidation
The
Company’s consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the
United States of America (“U.S. GAAP”). The consolidated financial statements include all accounts of the Company and its
majority owned and controlled subsidiaries. The Company consolidates entities in which it owns more than 50% of the voting common stock
and controls operations. All intercompany transactions and balances among consolidated subsidiaries have been eliminated. Non–controlling
interest represents the minority equity investment in the Company’s subsidiaries, plus the minority investors’ share of the
net operating results and other components of equity relating to the non–controlling interest.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
The
consolidated financial statements include all accounts of the entities as of the reporting period ending dates and for the reporting
periods as follows:
Schedule
of Condensed Financial Statements
Name of consolidated
subsidiary | |
State or other
jurisdiction of
incorporation or
organization | |
Date of incorporation
or formation | |
Attributable
interest as of
September 30, 2024 | | |
Attributable
interest as of
December 31, 2023 | |
| |
| |
| |
| | |
| |
Global BioMedical, Inc. | |
Nevada | |
April 18, 2017 | |
| 90.9 | % | |
| 90.9 | % |
Global BioLife, Inc. | |
Nevada | |
April 14, 2017 | |
| 81.8 | % | |
| 81.8 | % |
BioLife Sugar, Inc | |
Nevada | |
April 23, 2018 | |
| 90.9 | % | |
| 90.9 | % |
Happy Sugar Inc | |
Nevada | |
August 17, 2018 | |
| 81.8 | % | |
| 81.8 | % |
Sweet Sense Inc. | |
Nevada | |
April 30, 2018 | |
| 95.5 | % | |
| 95.5 | % |
Global Sugar Solutions Inc. | |
Nevada | |
November 7, 2019 | |
| 100 | % | |
| 100 | % |
As
of September 30, 2024, and December 31, 2023, the aggregate noncontrolling interest was equity of $3,003,000 and $3,040,000,
respectively, which are separately disclosed on the Consolidated Balance Sheets.
Use
of estimates
The
preparation of consolidated financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that
affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities as of the dates of the balance
sheets and reported amounts of revenues and expenses during the reporting periods. Actual results could differ from these estimates.
Reclassifications
Costs
associate with Sales and marketing have been reclassed from Other operating expenses for the three and nine months ended September 30,
2023 to conform with current period presentation. Also, cost associated with Professional fees for the three and nine months ended September 30, 2023 and the nine
months September 30, 2024 have been reclassified to Research and development to conform with current period presentation.
Loss
per Share
Basic
loss per share is computed by dividing the net loss attributable to the common stockholders by weighted average number of shares of common
stock outstanding during the period. Fully diluted loss per share is computed like basic loss per share except that the denominator is
increased to include the number of additional common shares that would have been outstanding if the potential common shares had been
issued and if the additional common shares were dilutive. There were no dilutive financial instruments issued or outstanding for the
three and nine months ended September 30, 2023. For the three and nine months ending September 30, 2024, there are 60,496,041 shares of Series A Convertible Preferred
Shares which are not eligible for conversion until April 10, 2027.
Fair
Value of Financial Instruments
Fair
value is defined as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between
market participants at the measurement date. The Fair Value Measurement Topic of the Financial Accounting Standards Board (“FASB”)
Accounting Standards Codification (“ASC”) establishes a three-tier fair value hierarchy which prioritizes the inputs used
in measuring fair value. The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical assets
or liabilities (Level 1 measurements) and the lowest priority to unobservable inputs (Level 3 measurements). These tiers include:
●
Level 1, defined as observable inputs such as quoted prices for identical instruments in active markets,
●
Level 2, defined as inputs other than quoted prices in active markets that are either directly or indirectly observable such as quoted
prices for similar instruments in active markets or quoted prices for identical or similar instruments in markets that are not active;
and
●
Level 3, defined as unobservable inputs in which little or no market data exists, therefore requiring an entity to develop its own assumptions,
such as valuations derived from valuation techniques in which one or more significant inputs or significant value drivers are unobservable.
The
carrying amounts reported in the balance sheet of cash and cash equivalents, prepaids, accounts payable and accrued expenses approximate
fair value because of the immediate or short-term maturity of these financial instruments. The fair value of notes receivable approximates
their carrying value as the stated or discounted rates of the notes do reflect recent market conditions. The Company’s investments
are recorded at cost as the fair value of these investment in is not readily available. The fair value of notes payable approximates
its carrying value as the stated interest rate reflects recent market conditions.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Cash
and cash equivalents
The
Company considers all highly liquid investments with a maturity of three months or less at the date of acquisition to be cash equivalents.
There were no cash equivalents as of September 30, 2024 and December 31, 2023.
Notes
receivable, unearned interest, and related recognition
The
Company records all future payments of principal and interest on notes as notes receivable, which are then offset by the amount of any
related unearned interest income. For financial statement purposes, the Company reports the net investment in the notes receivable on
the consolidated balance sheet as current or long-term based on the maturity date of the underlying notes. Such net investment is comprised
of the amount advanced on the loans, adjusting for net deferred loan fees or costs incurred at origination, amounts allocated to warrants
received upon origination, and any payments received in advance, if applicable. The unearned interest is recognized over the term of
the notes and the income portion of each note payment is calculated so as to generate a constant rate of return on the net balance outstanding.
If applicable, any net deferred loan fees or costs, together with discounts recognized in connection with warrants acquired at origination,
are accreted as an adjustment to yield over the term of the loan. (Note 3)
Goodwill
Goodwill
is the excess of cost of an acquired entity over the fair value of amounts assigned to assets acquired and liabilities assumed in a business
combination. Goodwill is subject to impairment testing at least annually and will be tested for impairment between annual tests, which
will take place during the fourth quarter in 2024, if an event occurs or circumstances change that would indicate the carrying amount
may be impaired. FASB ASC Topic 350 provides an entity with the option to first assess qualitative factors to determine whether the existence
of events or circumstances leads to a determination that it is more likely than not that the fair value of a reporting unit is less than
its carrying amount. Some of the qualitative factors considered in applying this test include consideration of macroeconomic conditions,
industry and market conditions, cost factors affecting the business, and overall financial performance of the business. If, after completing
the assessment, it is determined that it is more likely than not that the fair value of a reporting unit is less than its carrying value,
the Company will proceed to a quantitative test. If qualitative factors are not deemed sufficient to conclude that the fair value of
the reporting unit more likely than not exceeds its carrying value, then a one-step approach is applied in making an evaluation. The
evaluation utilizes an income approach (discounted cash flow analysis). The computations require management to make significant estimates
and assumptions, including, among other things, selection of comparable publicly traded companies, the discount rate applied to future
earnings reflecting a weighted average cost of capital, and earnings growth assumptions. The Company believes the estimates and assumptions
used in our impairment assessments are reasonable and based on available market information, but variations in any of the assumptions
could result in materially different calculations of fair value and determinations of whether or not an impairment is indicated. A discounted
cash flow analysis requires management to make various assumptions about future sales, operating margins, capital expenditures, working
capital, and growth rates. Cash flow projections are derived from one-year budgeted amounts plus an estimate of later period cash flows,
all of which are determined by management. Subsequent period cash flows are developed for each reporting unit using growth rates that
management believes are reasonably likely to occur. Impairment of goodwill is measured as the excess of the carrying amount of goodwill
over the fair values of recognized and unrecognized assets and liabilities of the reporting unit. No impairment was recognized during
the three or nine months ended September 30, 2024 and 2023. (Note 5)
Intangible
Assets
The
estimated fair values of acquired intangibles are generally determined based upon future economic benefits such as earnings and cash
flows. Acquired identifiable intangible assets are recorded at fair value and are amortized over their estimated useful lives. Acquired
intangible assets with an indefinite life are not amortized but are reviewed for impairment at least annually as of December 31st,
or more frequently whenever events or changes in circumstances indicate that the carrying amounts of those assets are below their estimated
fair values. Impairment is tested under ASC 350. No impairment was recognized for the three or nine months ended September 30, 2024,
and 2023. (Note 6)
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Recoverability
of Long-Lived Assets
We
evaluate long-lived assets such as property, equipment and definite lived intangible assets, such as patents, for impairment whenever
events or circumstances indicate that the carrying value of the assets recognized in our financial statements may not be recoverable.
Factors that we consider include whether there has been a significant decrease in the market value of an asset, a significant change
in the way an asset is being utilized, or a significant change, delay or departure in our strategy for that asset, or a significant change
in the macroeconomic environment. Our assessment of the recoverability of long-lived assets involves significant judgment and estimation.
These assessments reflect our assumptions, which, we believe, are consistent with the assumptions hypothetical marketplace participants
use. Factors that we must estimate when performing recoverability and impairment tests include, among others, forecasted revenue, margin
costs and the economic life of the asset. If impairment is indicated, we determine if the total estimated future cash flows on an undiscounted
basis are less than the carrying amounts of the asset or assets. If so, an impairment loss is measured and recognized.
Our
impairment loss calculations require that we apply judgment in identifying asset groups, estimating future cash flows, determining asset
fair values, and estimating asset’s useful lives. The Company reviews identifiable amortizable intangible assets for impairment
whenever events or changes in circumstances indicate that the carrying value of the assets may not be recoverable. Determination of recoverability
is based on the lowest level of identifiable estimated undiscounted cash flows resulting from use of the asset and its eventual disposition.
Measurement of any impairment loss is based on the excess of the carrying value of the asset over its fair value. Based on the uncertainty
of forecasts inherent with a new product, events such as the failure to generate forecasted revenue from new products could result in
a non-cash impairment in future periods.
Derivative Accounting
The Company analyzes all financial instruments with
features of both liabilities and equity under ASC 480, “Distinguishing Liabilities from Equity” and ASC 815, “Derivatives
and Hedging”. Derivative liabilities are adjusted to reflect fair value at each period end, with any increase or decrease
in the fair value being recorded in results of operations as adjustments to fair value of derivatives. The effects of interactions between
embedded derivatives are calculated and accounted for in arriving at the overall fair value of the financial instruments. Also, the fair
value of freestanding derivative instruments such as warrant and option derivatives are valued using the Black-Scholes simulation
model. The Company has determined that Note payable, related party contains an embedded derivative in the form of payment via equity and
has accounted for it in accordance with ASC 815. (see Note 7).
Revenue
Recognition
The
Company has adopted ASC Topic 606, Revenue from Contracts with Customers (“Topic 606”). The Company enters
into licensing and development agreements with collaborators for the development of its technologies. The terms of these agreements contain
multiple performance obligations which may include (i) licenses, or options to obtain licenses, to the Company’s technology, (ii)
rights to future technological improvements, and/or (iii) research activities to be performed on behalf of the collaborative partner.
Payments to the Company under these agreements may include upfront fees, option fees, exercise fees, payments based upon the achievement
of certain milestones, and royalties on product sales. Revenue is recognized when a customer obtains control of promised goods or services,
in an amount that reflects the consideration which the entity expects to receive in exchange for those goods or services. In determining
the appropriate amount of revenue to be recognized as it fulfills its obligations under the agreements, the Company performs the following
steps: (i) identification of the promised goods or services in the contract; (ii) determination of whether the promised goods or services
are performance obligations including whether they are distinct in the context of the contract; (iii) measurement of the transaction
price, including the constraint on variable consideration; (iv) allocation of the transaction price to the performance obligations; and
(v) recognition of revenue when or as the Company satisfies each performance obligation.
The
Company only applies the five-step model to contracts when it is probable that the Company will collect the consideration to which it
is entitled in exchange for the goods or services it transfers to the customer. At contract inception, once the contract is determined
to be within the scope of ASC 606, the Company assesses the goods or services promised within each contract and determines those that
are performance obligations and assesses whether each promised good or service is distinct. The Company then recognizes as revenue the
amount of the transaction price that is allocated to the respective performance obligation when or as the performance obligation is satisfied.
Research
and Development
Research
and development costs are expensed as incurred. Total research and development costs were $386,000 for the nine months ended September
30, 2024, and $1,055,000 for nine months ended September 30, 2023.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Provision
for Credit Losses
On
January 1, 2022, the Company adopted amended accounting guidance “ASU No.2016-13 – Credit Losses” which requires
an allowance for credit losses to be deducted from the amortized cost basis of financial assets to present the net carrying value at
the amount that is expected to be collected over the contractual term of the asset considering relevant information about past events,
current conditions, and reasonable and supportable forecasts that affect the collectability of the reported amount. In estimating expected
losses in the loan and lease portfolio, borrower-specific financial data and macro-economic assumptions are utilized to project losses
over a reasonable and supportable forecast period. Assumptions and judgment are applied to measure amounts and timing of expected future
cash flows, collateral values and other factors used to determine the borrowers’ abilities to repay obligations. After the forecast
period, the Company utilizes longer-term historical loss experience to estimate losses over the remaining contractual life of the loans.
Prior to 2022, the allowance for credit losses represented the amount that in management’s judgment reflected incurred credit losses
inherent in the loan and lease portfolio as of the balance sheet date. As of September 30, 2024 and December 31, 2023 the Company has
deemed that no reserve on credit losses were necessary.
Continuing
Operations and Going Concern
The
accompanying consolidated financial statements have been prepared assuming that the Company will continue as a going concern. This basis
of accounting contemplates the recovery of our assets and the satisfaction of liabilities in the normal course of business. As reflected
in the accompanying financial statements the Company has incurred operating losses as well as negative cash flows from operating and
investing activities over the past two years. These factors raise substantial doubt about the Company’s ability to continue as
a going concern within one year of the date that the financial statements are issued. These consolidated financial statements do not
include any adjustments to the specific amounts and classifications of assets and liabilities, which might be necessary should we be
unable to continue as a going concern.
To
continue as a going concern, the Company completed an initial public offering on September 16, 2024 raising $3,726,000
net of issuance costs and is currently listed on the NYSE American under the ticker symbol IBIO. The Company’s management
intends to take additional actions necessary to continue as a going concern. Management’s plans concerning these matters include,
among other things, monetization of its intellectual properties, and tightly controlling operating costs.
Recent
Accounting Standards
The
Financial Accounting Standards Board (FASB) issues various Accounting Standards Updates relating to the treatment and recording of certain
accounting transactions. There are several new accounting pronouncements issued by FASB which are not yet effective. Each of these pronouncements,
as applicable, has been or will be adopted by the Company. As of September 30, 2024, none of these pronouncements are expected to have
a material effect on the financial position, results of operations or cash flows of the Company.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Note
3. Notes Receivable
On
February 19, 2021, Impact BioMedical, Inc, entered into a promissory note with an individual. The Company loaned the principal sum of
$206,000, with interest at a rate of 6.5%, and maturity date of August 19, 2022 later amended to February 19, 2026. Monthly payments
are due on the twenty-first day of each month and continuing each month thereafter until February 19, 2026. This note is secured by certain
real property situated in Collier County, Florida. The outstanding principal and interest as of September 30, 2024 and December 31, 2023,
was approximately $201,000 and $203,000, respectively. At September 30, 2024, $142,000 is classified in Current notes receivable and
the remaining $59,000 is classified as Notes receivable on the accompanying consolidated balance sheets. At December 31, 2023, $203,000
is classified in Current notes receivable.
Note
4. Property, Plant and Equipment, Net
Property,
plant and equipment consisted of the following as of:
Schedule
of Property Plant and Equipment
| |
Estimated | |
September 30, | | |
December 31, | |
| |
Useful Life | |
2024 | | |
2023 | |
Machinery and equipment | |
5-10 years | |
$ | 30,000 | | |
$ | 30,000 | |
Construction in progress | |
| |
| 263,000 | | |
| 263,000 | |
Total Cost | |
| |
| 293,000 | | |
| 293,000 | |
Less accumulated depreciation | |
| |
| 11,000 | | |
| 6,000 | |
Property, plant and equipment, net | |
| |
$ | 282,000 | | |
$ | 287,000 | |
Depreciation
expense for the nine months ended September 30, 2024 and 2023 was approximately $5,000 and $4,000, respectively.
Note
5. Goodwill
Goodwill
balances and activity for the nine months ended September 30, 2024 and year ended December 31, 2023 consisted of the following:
Schedule
of Goodwill
| |
| | |
Balance at December 31, 2023 | |
$ | 25,093,000 | |
Goodwill adjustment | |
| - | |
Balance at September 30, 2024 | |
$ | 25,093,000 | |
As
of September 30, 2023, management performed annual goodwill impairment testing. No goodwill impairment was identified as a result of
these tests. As of September 30, 2023, a quantitative analysis was prepared utilizing the Market Approach and Income Approach valuing
the Company. The guideline public company Market Approach produced a mean business enterprise value indication using estimated 2026 results
of $49.8 million. The Income Approach was based upon the use of a discounted pro forma cash flow model and produced a business enterprise
value indication of $44.9 million. A weighting of 30% to the weighted value indicated was applied under the Market Approach, and a weighting
of 70% to the value indicated under the Income Approach. A lower weighting was applied to the Market Approach due to the fact of using
forecasted earnings of the Company. Based upon the above weightings, an initial value of $46.4 million for Impact was calculated. Adding
cash of $201,000 to the initial business enterprise value produced a concluded business enterprise value of $46.6 million (rounded) for
Impact. Subtracting interest-bearing debt of $11.9 million, results in a Fair Value for the common equity of Impact of $34.7 million.
As of September 30, 2023, the indicated equity value exceeded the carrying amount by approximately $5.1 million or 14.7%. No circumstances
or events have occurred since the most recent analysis that would indicate the need for an impairment.
Note
6. Intangible Assets
The
definite-lived intangible assets, to be amortized over 20 years, balances, and activity for the nine months ended September 30, 2024
and year ended December 31, 2023 consisted of the following:
Schedule
of Intangible Assets
| |
September 30, 2024 | | |
December 31, 2023 | |
| |
Gross
Carrying Amount | | |
Accumulated Amortization | | |
Net
Carrying Amount | | |
Gross
Carrying Amount | | |
Accumulated Amortization | | |
Net
Carrying Amount | |
Definitive-lived: | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Developed technology | |
$ | 22,260,000 | | |
$ | (4,174,000 | ) | |
$ | 18,086,000 | | |
$ | 22,260,000 | | |
$ | (3,339,000 | ) | |
$ | 18,921,000 | |
Total | |
$ | 22,260,000 | | |
$ | (4,174,000 | ) | |
$ | 18,086,000 | | |
$ | 22,260,000 | | |
$ | (3,339,000 | ) | |
$ | 18,921,000 | |
Amortization
expense for the nine months ended September 30, 2024 and 2023 was approximately $835,000 and $835,000, respectively.
The
following table represents future amortization of developed technologies for the years ending December 31:
Schedule
of Future Amortization of Developed Technologies
| |
| | |
2024 | |
$ | 279,000 | |
2025 | |
$ | 1,113,000 | |
2026 | |
$ | 1,113,000 | |
2027 | |
$ | 1,113,000 | |
2028 | |
$ | 1,113,000 | |
Thereafter | |
$ | 13,355,000 | |
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Note
7. Note payable, related party
On
December 31, 2020, and later amended, the Company executed a Revolving Promissory Note (“Note”) with DSS, a related
party, which accrues interest at a rate of 4.25%
and is due in full at the maturity date of September
30, 2030. The Note was further amended on July 24, 2024 with an effective date of September 16, 2024 to i) allow the Company
to pay certain principal and/or interest payments owing under the repayment terms in an exchange for potential of equity in the
Company, ii) change the quarterly interest due dates to the last day of each calendar quarter (i.e. December 31, March 31, June 30
and September 30), iii) to adjust the On Demand feature so that it starts after the 24th month, iv) continue the planned repayment program commencing on the 37th month and
on the last day of each month thereafter through August 31, 2030 to pay a fixed monthly payment of $126,381,
v) to continue the scheduled maturity date of September 30, 2030, and vi) adjusts the interest rate to be the WSJ Prime Rate plus 0.50%.
As of September 30, 2024 and December 31, 2023 the outstanding balance, inclusive of interest was $8,006,000
(net of change in fair value of embedded derivative of $5,670,000)
and $12,074,000, respectively. Of
the $8,006,000,
$35,000
is included in Current portion of note payable, related party and the remaining $7,971,000
is included in Long-term portion of note payable, related party at September 30, 2024. The $12,074,000
at December 31, 2023 is included in Current portion of note payable, related party.
A
summary of scheduled principal payments of long-term debt (exclusive of the embedded derivative of $5,670,000), subsequent to September 30,
2024, are as follows:
Schedule
of Principal Payments of Long-term Debt
Year | | |
Amount | |
| 2024 | | |
$ | 35,000 | |
| 2025 | | |
| 781,000 | |
| 2026 | | |
| 12,860,000 | |
The
movement in the liability and derivative components of the Note payable, related party as of December 31,2023 and September 30, 2024
are set out below:
Schedule of Movement of Liability and
Derivative Components of Note Payable
| |
Liability Component | | |
Derivative Component | | |
Total | |
December 31, 2023 | |
$ | 12,074,000 | | |
$ | - | | |
$ | 12,074,000 | |
Change in fair value of embedded derivative | |
| (7,098,000 | ) | |
| 1,428,000 | | |
| (5,670,000 | ) |
Advances on note | |
| 807,000 | | |
| - | | |
| 807,000 | |
Interest expense | |
| 795,000 | | |
| - | | |
| 795,000 | |
September 30, 2024 | |
$ | 6,578,000 | | |
$ | 1,428,000 | | |
$ | 8,006,000 | |
We
considered various valuation methodologies in our analysis of the embedded derivative. Valuation methodologies can generally be aggregated
into the following three approaches: the Market Approach, the Income Approach, and the Cost Approach. Based on our analysis of the facts
and circumstances, in estimating the fair value of the Note payable, related party, we utilized a discounted cash flow method (income
approach), in the form of a Monte Carlo simulation of the Company’s stock price and volume weighted average price (“VWAP”)
throughout 36-month period from the Effective Date relative to its closing stock price and VWAP as of the Valuation Date, or $2.00 and
$2.38, respectively. The simulated analysis estimates the expected note cash flow from the date the first payment is due and until the
equity conversion rights expire under the terms of the Note payable, related party based on the following steps:
1) | Developed
the Note Payable repayment schedule |
2) | Developed
the following inputs underlying the simulation analysis |
3) | Inputs
(i) and (ii), were assigned a normal probability distribution, which has a mean of 0 and
a standard deviation of 1, and a correlation of .9885 based on analysis of the guideline
public companies |
4) | Ran
a simulation with 25,000 trials for purposes of capturing the key inputs discussed above
(i.e., forecasting the stock price and VWAP). |
5) | For
the period from the 37th payment to maturity date, the DCF Method includes the remaining
payments required to be made in cash. |
6) | Captured
the results of the simulation and concluded based on the simulation results |
Note 8. Financial Instruments
Cash, Note payable, related party
The following tables show the Company’s cash,
cash equivalents, restricted cash, and note payable, related party by significant investment category as of:
Schedule of Cash,
Cash Equivalents, Restricted Cash, and Note Payable Related Party by Significant Investment Category
| |
September 30, 2024 |
|
| |
Adjusted
cost | | |
Unrealized Gain/(Loss) | | |
Fair Value | | |
Cash and Cash Equivalents | |
|
Note
Payable,
Related Party |
|
Cash | |
$ | 2,668,000 | | |
$ | - | | |
$ | 2,668,000 | | |
$ | 2,668,000 | |
|
$ |
- |
|
Level 2 | |
| | | |
| | | |
| | | |
| | |
|
|
|
|
Note payble, related party | |
| 13,676,000 | | |
| (5,670,000 | ) | |
| 8,006,000 | | |
| - | |
|
|
8,006,000 |
|
Total | |
$ | 16,344,000 | | |
$ | (5,670,000 | ) | |
$ | 10,674,000 | | |
$ | 2,668,000 | |
|
$ |
8,006,000 |
|
| |
September 30, 2023 | |
| |
Adjusted Cost | | |
Unrealized Gain/(Loss) | | |
Fair Value | | |
Cash and Cash Equivalents | |
Cash | |
$ | 1,000 | | |
$ | - | | |
$ | 1,000 | | |
$ | 1,000 | |
Total | |
$ | 1,000 | | |
$ | - | | |
$ | 1,000 | | |
$ | 1,000 | |
Note
9. Stockholders’ Equity
On
May 10, 2023, the Company’s Board of Directors approved an amendment to the Articles of Incorporation of the Company to increase
the total number of shares of Common Stock to 4,000,000,000
shares with a par value of $0.001.
Each
share of Common Stock when issued, shall have one (1) vote on all matters presented to the stockholders. Our
Amended and Restated Articles of Incorporation also authorized 100,000,000
shares of preferred stock, par value $0.001
per share. On May 11, 2023, the Company effected
a forward split. As a result, there were 3,877,282,251
shares of our Common Stock and no
shares of preferred stock issued and outstanding.
Prior to the split, there were 125,073,621
shares of our Common Stock and no
shares of preferred stock issued and outstanding.
On October 31, 2023, the Company effected a reverse stock split of 1 for 55. Also on October 31, 2023, DSS BioHealth
Securities, Inc., the Company’s largest shareholder converted 60,496,041
shares of Common Stock into 60,496,041
shares of Series
A Convertible Preferred Shares, reducing its ownership of the Company’s Common Stock from approximately 88% to approximately 12%.
As of December 31, 2023, there were 10,000,000
shares of our Common Stock and 60,496,041
shares
of preferred stock issued and outstanding.
On
August 8, 2023 DSS, the Company’s largest shareholder, distributed to its shareholders of record on July 10, 2023 4 shares of Impact
Bio’s stock for 1 share they owned. Each share of Impact BioMedical distributed as part of the distribution will not be eligible
for resale until 180 days from the date Impact BioMedical’s initial public offering becomes effective under the Securities Act,
subject to the discretion of the Company to lift the restriction sooner.
On
October 31, 2023, the Company effected a reverse stock split of 1 for 55. As of December 31, 2023, and December 31, 2022, there were 3,877,282,251
shares of our Common Stock issued and outstanding which was converted to 70,496,041
shares. Also on October 31, 2023, DSS BioHealth Securities, Inc., the Company’s largest shareholder converted 60,496,041
shares of Common Stock into 60,496,041
shares of Series A Convertible Preferred
Shares, reducing its ownership of the Company’s Common Stock from approximately 88% to approximately 12%. The Series A
Convertible Preferred Shares are not eligible for conversion until April 10, 2027.
On
September 16, 2024, Impact Biomedical Inc., entered into an underwriting agreement (the “Underwriting Agreement”) with
Revere Securities, LLC., as representative (the “Representative”) of the underwriters named therein (the
“Underwriters”), pursuant to which the Company agreed to sell to the Underwriters in a firm commitment initial public
offering (the “Offering”) an aggregate of 1,500,000
of the Company’s shares of common stock, par value $0.001
per share at a public offering price of $3.00
per share. On September 17, 2024, the Company closed the Offering, and as of September 30, 2024 there were 11,503,955
shares of common stock issued and outstanding. The total net proceeds to the Company from the Offering, after deducting discounts,
expenses allowance and expenses, was approximately $3,726,000.
A final prospectus relating to this Offering was filed with the Commission on September 16, 2024. The shares of Common Stock were
approved to list on the NYSE American under the symbol “IBO” and began trading there on September 16, 2024. The Company
also issued warrants to the Representative and its affiliates (the “Representative’s Warrants”) warrants to
purchase the number of shares of Common Stock in the aggregate equal to 5%
of the Common Stock to be issued and sold in this offering (including any Shares of Common Stock sold upon exercise of the
over-allotment option, if applicable). The Representative’s Warrants are exercisable for a price per share equal to 125%
of the public offering price. The warrants are exercisable at any time, in whole or in part, commencing nine (9) months from the
date of commencement of sales of the offering and ending on the third anniversary thereof. As of September 30, 2024, the
Representative had not exercised any of these warrants. As of September 30, 2024, only the 1,500,000
shares included in the Offering are freely tradable on the NYSE. The remaining 9,997,703
are restricted from trading for 180 days from the Offering date.
Note
10. Related Party Transactions
Research
and Development Activities
Based
on a shareholders agreement entered into on April 26, 2017, the Company would fund the scientific operations of GRDG, a company involved
in research and development of biomedical products which is a minority stockholder of two of the Company’s subsidiaries and is
owned by Daryl Thompson, a former director of many subsidiaries of the Company, to do the development and research works on the biomedical
products for the Company. On February 15, 2022, the Company and its subsidiaries, Global BioLife, Inc. (“Global”), and Impact
BioLife Sciences, Inc. (“BioLife Sciences”), and GRDG entered into a Licensing Proceeds Distribution Agreement (“GRDG
Agreement”), whereas GRDG would transfer its 20% equity position in both Global and BioLife Sciences to the Company in exchange
for 20% interest in Global and/or BioLife Science revenue received from the exclusive or non-exclusive licensing of and/or the sale of
Global Intellectual Property to a Third Party, net of specific costs. As of the date of this report, no contingent liability has been
recognized under the GRDG Agreement. The research and development agreement as well as the licensing proceeds distribution agreement
with GRDG were terminated in 2023. As of September 30, 2023, the Company incurred approximately $258,000 in expenses, and had approximately
$25,000 in prepaid monthly fees. For the nine months ended September 30, 2024, the Company had incurred $25,000 in fees.
General
and Administrative Costs
There
are certain general and administrative costs incurred by DSS, a related party, on behalf of the Company which are passed through to the
Company on a monthly basis. These costs consist of primarily payroll costs for certain DSS employees and are allocated based on estimated
time spent on behalf of the Company. Beginning in January 2024, these costs are approximately $31,000 per month. As of September 30,
2024, the Company incurred approximately $265,000 in related expenses. As of September 30, 2023, the Company incurred approximately $108,000
in related expenses
Note
payable, related party
On December 31, 2020, and later amended, the Company
executed a Revolving Promissory Note (“Note”) with DSS, a related party, which accrues interest at a rate of 4.25% and is
due in full at the maturity date of September 30, 2030. The Note was further amended on July 24, 2024 with an effective date of September
16, 2024 to i) allow the Company to pay certain principal and/or interest payments owing under the repayment terms in an exchange of equity
in the Company, ii) change the quarterly interest due dates to the last day of each calendar quarter (i.e. December 31, March 31, June
30 and September 30), iii) to partially eliminate the “On Demand, if No Demand” feature so that the “On Demand, if
no Demand” feature only starts after the 24th month, iv) continue the planned repayment program commencing on the 37th month and
on the last day of each month thereafter through August 31, 2030 to pay a fixed monthly payment of $126,381,
v) to continue the scheduled maturity date of September 30, 2030, and vi) adjusts the interest rate to be the WSJ Prime Rate plus 0.50%.
As of September 30, 2024 and December 31, 2023 the outstanding balance, inclusive of interest was $8,006,000 (net of change in fair value
of embedded derivative of $5,670,000) and $12,074,000, respectively. Of the $8,006,000, $35,000 is included in Current portion of note
payable, related party and the remaining $7,971,000 is included in Long-term portion of note payable, related party at September
30, 2024. The $12,074,000 at December 31, 2024 is included
in Current portion of note payable, related party (see Note 7).
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Note
11. Commitments and Contingencies
On
August 15, 2018, the Company entered into Royalty Agreement with Chemia Corporation (“Chemia”) pursuant to which Chemia transferred
to the Company all of its right to 3F (Functional Fragrance Formulation). This agreement has a 20-year term and auto renews for a period
of 1 year unless mutually agreed upon by both parties. 3F consists of 3F Mosquito Repellant and 3F Anti-Viral formulations. Based on
the Royalty Agreement, the Company should cover all the costs to prepare and finalize necessary patent application and other intellectual
property related to 3F. Chemia agreed to support the Company in efforts leading to development of 3F intellectual property and it is
licensing. Based on Royalty Agreement any payments received from development, sales, licensing or transfer of 3F technology will be paid
50% to the Company and 50% to Chemia. On November 27, 2018, Company and Chemia signed an Addendum to Royalty Agreement (“Addendum”),
according to which the Company granted Chemia a royalty-based limited license for purposes of making and selling fragrances embodying
the 3F technology. Based on the Addendum, Chemia should pay the Company 5% of net sales in royalty. On November 8, 2019, both companies
entered into Amendment no.1 to Royalty Agreement, based on which certain expenses borne by the Company towards patent application and
licensing should be reimbursed to the Company before any royalty payments are made. For the three and nine months ended September 30,
2024 and 2023, there were no reimbursements or royalties paid to the Company and the Company cannot be assured that Chemia’s efforts
will end up in any future sales of the technology.
On
February 15, 2022, the Company and its subsidiaries, Global BioLife, Inc. (“Global”), and Impact BioLife Sciences, Inc. (“BioLife
Sciences”), and GRDG entered into a Licensing Proceeds Distribution Agreement (“GRDG Agreement”), whereas GRDG would
transfer its 20% equity position in both Global and BioLife Sciences to the Company in exchange for 20% interest in Global and/or BioLife
Science revenue received from the exclusive or non-exclusive licensing of and/or the sale of Global Intellectual Property to a Third
Party, net of specific costs. This Licensing Agreement ended in September 2023 as core technologies achieved significant development
milestones.
On
March 19, 2022, Impact BioMedical entered into a License Agreement (“Equivir License”) with a third-party (“Licensee”)
where the Licensor is granted the right, amongst other things, to develop, commercialize, and sell the Company’s Equivir technology.
In exchange, the Licensee shall pay the Company a royalty of 5.5% of net sales. Under the terms of the Equivir Agreement, the Company
shall reimburse the Licensee for 50% of the development costs provided that the development costs shall not exceed $1,250,000. As of
September 30, 2024 and December 31, 2023, a liability of $0 and $200,000, respectively, has been recorded in relation to the Equivir
License.
Note
12. Subsequent Events
The
Company has evaluated all other subsequent events and transactions through November 12, 2024, the date that the consolidated financial
statements were available to be issued and noted no other subsequent events requiring financial statement recognition or disclosure.
ITEM
2 - MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
FORWARD-LOOKING
STATEMENTS
Certain
statements contained herein this report constitute “forward-looking statements” within the meaning of the Private Securities
Litigation Reform Act of 1995 (the “1995 Reform Act”). Except for the historical information contained herein, this report
contains forward-looking statements (identified by words such as “estimate,” “project”, “anticipate”,
“plan”, “expect”, “intend”, “believe”, “hope”, “strategy” and
similar expressions), which are based on our current expectations and speak only as of the date made. These forward-looking statements
are subject to various risks, uncertainties and factors that could cause actual results to differ materially from the results anticipated
in the forward-looking statements.
Overview
Impact
BioMedical, Inc. (the “Company”, “Impact BioMedical”, “We”) through the utilization of its intellectual
property rights, or through investment in, or through acquisition of companies in the biohealth and biomedical fields, focuses on the
advancement of drug discovery and prevention, inhibition, and treatment of neurological, oncological, and immune related diseases. The
Company is also developing open-air defense initiatives, which curb transmission of air-borne infectious diseases, such as tuberculosis
and influenza.
Global
BioLife, Inc. (“Global BioLife”), one of the Company’s subsidiaries and the main operating company of the group, focuses
on research in four main areas: (i) the “Linebacker” project, which aims to develop a universal therapeutic drug platform;
(ii) a new sugar substitute called “Laetose,”; (iii) a multi-use fragrance called “3F” (Functional Fragrance
Formulation); and (iv) Equivir/Nemovir, a blend of natural polyphenols designed as an antimicrobial medication.
Linebacker
Unlike
the traditional approach to treat individual diseases with specific drugs, the Linebacker platform seeks to offer a breakthrough therapeutic
option for multiple diseases. Linebacker is designed to work by inhibiting a cascade of inflammatory responses responsible for many diseases.
Its design is in direct contrast to the traditional approach of targeting individual diseases with specific drugs.
Laetose
We
have also developed a low-calorie, low glycemic level, natural modified sugar through Global BioLife. The product, “Laetose,”
is designed to possess low glycemic properties and mitigate inflammation. The Company is presently seeking to license Laetose. Global
BioLife established a joint venture, Sweet Sense, Inc. (“Sweet Sense”), with Quality Ingredients, LLC for the development,
manufacture, and global distribution of the new sugar substitute. On November 8, 2019, the Company purchased 50% of Sweet Sense Inc.
from Quality Ingredients, LLC for $91,000. Sweet Sense is now an 81.8% owned subsidiary of Impact BioMedical.
Functional
Fragrance Formulation (“3F”)
Global
BioLife has entered into a royalty agreement with U.S.-based Chemia Corporation (“Chemia”), a leading developer and manufacturer
of fragrances, to manufacture the 3F technology. This arrangement, under the terms of the agreement, allows Chemia to create fragrances
based on Global BioLife’s patents. The 3F product is made from specialized oils sourced from botanicals that insects avoid. Global
BioLife aims to commercialize this product, with any potential profits from the 3F project being split between Global BioLife and Chemia
pursuant to the terms of the 20-year Royalty Agreement. (Note 10)
Equivir
Equivir,
is a polyphenol compound that is believed to be successful in antiviral infection treatments. Equivir is a patented medication, which
has broad antiviral efficacy against multiple types of infectious disease.
The
Company was incorporated in the State of Nevada as a for-profit company on October 16, 2018 and established a fiscal year end of December
31st. The Company issued 9,000 shares to its sole shareholder Global BioMedical Pte. Ltd., which was wholly owned by Alset International
Limited (formally Singapore eDevelopment Limited), a multinational public company, listed on the Singapore Exchange Securities Trading
Limited (“SGXST”). On March 31, 2020, the Company issued 125,064,621 shares of common stock to its sole shareholder Global
BioMedical Pte. Ltd. On July 24, 2020, the Board approved the Stock Split, pursuant to which each share of the Company’s common
stock issued and outstanding was split into nine shares of the Company’s common stock. The numbers of authorized common stock and
issued and outstanding common stock in the reporting periods were retrospectively adjusted for the stock split.
Impact
BioMedical, Inc. targets unmet, urgent medical needs and expands the borders of medical and pharmaceutical science. Impact drives mission-oriented
research, development, and commercialization of solutions for medical advances in human wellness and healthcare. By leveraging technology
and new science with strategic partnerships, Impact Bio provides advances in drug discovery for the prevention, inhibition, and treatment
of neurological, oncology and immuno-related diseases. Other exciting technologies include a breakthrough alternative sugar aimed to
combat diabetes and functional fragrance formulations aimed at the industrial and medical industry.
The
business model of Impact BioMedical revolves around two methodologies – Licensing and Sales Distribution:
1)
Impact develops valuable and unique patented technologies which will be licensed to pharmaceutical, large consumer package goods
companies and venture capitalists in exchange for usage licensing and royalties.
2)
Impact utilizes the DSS ecosystem to leverage its sister companies that have in place distribution networks on a global scale. Impact
will engage in branded and private labelling of certain products for sales generation through these channels. This global distribution
model will give direct access to end users of Impact’s nutraceutical and health related products.
Costs
and expenses
| |
Three months ended September 30, 2024 | | |
Three months ended September 30, 2023 | | |
% Change | | |
Nine months ended September 30, 2024 | | |
Nine months ended September 30,2023 | | |
% Change | |
| |
| | |
| | |
| | |
| | |
| | |
| |
Sales, general and administrative compensation | |
| 132,000 | | |
| 101,000 | | |
| 31 | % | |
| 424,000 | | |
| 182,000 | | |
| 133 | % |
Sales and marketing | |
| 461,000 | | |
| 17,000 | | |
| 2612 | % | |
| 487,000 | | |
| 44,000 | | |
| 1007 | % |
Professional Fees | |
| 122,000 | | |
| 317,000 | | |
| -62 | % | |
| 313,000 | | |
| 750,000 | | |
| -58 | % |
Research and development | |
| 82,000 | | |
| 357,000 | | |
| -77 | % | |
| 386,000 | | |
| 1,055,000 | | |
| -63 | % |
Depreciation and Amortization | |
| 281,000 | | |
| 280,000 | | |
| 0 | % | |
| 840,000 | | |
| 840,000 | | |
| 0 | % |
Rent and utilities | |
| 4,000 | | |
| - | | |
| N/A | | |
| 14,000 | | |
| - | | |
| N/A | |
Other operating expenses | |
| 45,000 | | |
| 6,000 | | |
| 650 | % | |
| 58,000 | | |
| 18,000 | | |
| 222 | % |
| |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Total costs and expenses | |
$ | 1,127,000 | | |
$ | 1,078,000 | | |
| 5 | % | |
$ | 2,522,000 | | |
$ | 2,889,000 | | |
| -13 | % |
Selling,
general and administrative compensation costs increased 31% for the three months ended September 30, 2024, as compared to the
three months ended September 30, 2023 and increased 133% for the nine months ended September 30, 2024, as compared to the nine months
ended September 30, 2023 due to increased cost incurred associated with the Company’s registration with the SEC and the NYSE
American, and efforts toward the Company’s IPO.
Sales
and marketing costs, which includes internet and trade publication advertising, press releases, travel and entertainment costs.
These increased 2,612% for the three months ended September 30, 2024, as compared to the three months ended September 30, 2023 and
decreased 1,007% for the nine months ended September 30, 2024, as compared to the nine months ended September 30, 2023. The increase
in cost for the three and nine months ended September 30, 2024 are associated with cost to attend trade shows and marketing efforts pre and post IPO.
Professional
fees decreased 62% for the three months ended September 30, 2024, as compared
to the three months ended September 30, 2023 and decreased 58% for the nine months ended September 30, 2024, as compared to the nine months
ended September 30, 2023. These cost consist primarily of consulting and legal services associated with developing and implementing Impact
BioMedical’s business plan, These costs decreased in 2024 in anticipation of the Company’s IPO.
Research
and development costs represent costs consisting primarily of independent, third-party testing of the various properties of each
technology the Company owns possesses, research on new technologies as well as cost to patent newly developed technologies and other
related fees for the development of new technologies. Research and development decreased 100% for the three months ended September 30, 2024, as
compared to the three months ended September 30, 2023 and decreased 93% for the nine months ended September 30, 2024, as compared to
the nine months ended September 30, 2023, due primarily to the cessation of the Company’s research and development contract
with GRDG at the end of 2023.
Depreciation
and amortization expense is flat for the three and nine months ended September 30, 2024 as
compared to September 30, 2023 and represents the amortization of the associated with the developed technology and patents acquired as
part of the acquisition of Impact BioMedical by DSS.
Rent
and utilities represents cost associated with office space located at 1400 Broadfield Blvd, Suite 100 Houston TX which the Company
began subletting from DSS during the first quarter of 2024.
Other
operating expenses consist primarily of office supplies, IT support, sales and marketing costs,
travel and insurance costs. These costs increased 650% for the three months ended September 30, 2024, as compared to the three months
ended September 30, 2023 and increased 222% for the nine months ended September 30, 2024, as compared to the nine months ended September
30, 2023.
Other
Income (Expense)
| |
Three months ended September 30, 2024 | | |
Three months ended September 30, 2023 | | |
% Change | | |
Nine months ended September 30, 2024 | | |
Nine months ended September 30,2023 | | |
% Change | |
| |
| | |
| | |
| | |
| | |
| | |
| |
Interest income | |
$ | 3,000 | | |
$ | 3,000 | | |
| 0 | % | |
$ | 10,000 | | |
$ | 10,000 | | |
| 0 | % |
Other income | |
| - | | |
| - | | |
| N/A | | |
| - | | |
| 52,000 | | |
| -100 | % |
Change in fair value of embedded derivative | |
| 5,670,000 | | |
| - | | |
| N/A | | |
| 5,670,000 | | |
| - | | |
| N/A | |
Interest expense | |
| (305,000 | ) | |
| (102,000 | ) | |
| 199 | % | |
| (795,000 | ) | |
| (319,000 | ) | |
| 149 | % |
| |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Total other income(expense) | |
$ | 5,368,000 | | |
$ | (99,000 | ) | |
| 5522 | % | |
$ | 4,885,000 | | |
$ | (257,000 | ) | |
| 2001 | % |
Interest
income is recognized on the Company’s notes receivable. Interest income
was flat for three and nine months ended September 30, 2024 as compared to September 30, 2023 as the outstanding principal balance remained
flat.
Other
income represents income generated from the Company’s distribution agreement with BioMed Technologies (“BioMed”).
during the first quarter of 2023. BioMed’s products focus on natural probiotics.
Change in fair value of embedded derivative is related to the promissory
note with DSS which allows the Company to repay both principal and interest with common stock of the Company.
Interest
expense is recognized on the Company’s debt to DSS. Interest expense increased
199% and 149% for three and nine months ended September 30, 2024 as compared to September 30, 2023, respectively, due to the increased
outstanding balance of debt due.
Net
Income (Loss)
| |
Three months ended September 30, 2024 | | |
Three months ended September 30, 2023 | | |
% Change | | |
Nine months ended September 30, 2024 | | |
Six months ended September 30, 2023 | | |
% Change | |
| |
| | |
| | |
| | |
| | |
| | |
| |
Net income (loss) | |
$ | 4,450,000 | | |
$ | (1,177,000 | ) | |
| 478 | % | |
$ | 2,572,000 | | |
$ | (3,146,000 | ) | |
| 182 | % |
For
the three and nine months ended September 30, 2024 and 2023, the Company recorded increases in net income (loss) of 478% and 182%,
respectively. The increase in net income (loss) is attributable to the Company’s cost cutting measures in taken with both its
professional and research and development costs as the Company shifts efforts to taking to market its existing technologies as well
as the change in fair value of embedded derivatives associated with the amended Note payable, related party.
LIQUIDITY
AND CAPITAL RESOURCES
The
Company has historically met its liquidity and capital requirements primarily through debt financing. On September 16, 2024, the Company
completed an initial public offering raising $3,726,000 net of issuance costs and is currently listed on the NYSE American under the
ticker symbol IBIO. The Company’s management intends to take additional actions necessary to continue as a going concern. Management’s
plans concerning these matters include, among other things, monetization of its intellectual properties, and tightly controlling operating
costs.
Cash
Flow from Continuing Operating Activities
Net cash used by operating activities was $2,663,000 for the nine months
ended September 30, 2024 as compared to cash used by operating activities of $2,418,000 for the nine months ended September 30, 2023.
This fluctuation is driven by less payments of the Company’s accounts payable by approximately $232,000, as well as decrease in
net loss after reconciling items of approximately $161,000
Cash
Flow from Investing Activities
Net
cash provided by investing activities was $2,000 for the nine months ended September 30, 2024 as compared to cash used by investing
activities of $16,000 for the nine months ended September 30, 2023. This fluctuation is driven by the purchase of capital assets
approximating $18,000 during the nine months ended September 30, 2023 without similar activities during 2024.
Cash
Flow from Financing Activities
Net
cash provided by financing activities was $5,328,000 for the nine months ended September 30, 2024 and represents $1,602,000 in
borrowings from DSS as well as $3,726,000 in issuance of common stock, net of issuance costs. During the nine months ended
September 30, 2023, net cash provided by financing activities was driven by borrowings from DSS of $2,633,000.
Off-Balance
Sheet Arrangements
We
do not have any material off-balance sheet arrangements that have, or are reasonably likely to have, an effect on our financial condition,
financial statements, revenues, or expenses.
Critical
Accounting Policies and Estimates
The
preparation of financial statements and related disclosures in conformity with U.S. GAAP requires management to make judgments,
assumptions and estimates that affect the amounts reported in our financial statements and accompanying notes. The financial
statements as of December 31, 2023, describe the significant accounting policies and methods used in the preparation of the
financial statements. Accounting for derivatives has been added to Footnote 2 of the accompanying financial statements. There are
no additional material changes to such critical accounting policies as of the Quarterly Report on Form 10-Q for the quarter ended
September 30, 2024.
ITEM
4 - CONTROLS AND PROCEDURES
Under
the supervision and with the participation of our management, including our principal executive officer and principal financial officer,
we conducted an evaluation of our disclosure controls and procedures for the quarter ended September 30, 2024, pursuant to Rule 13a-15(e)
and Rule 15d-15(e) promulgated under the Securities Exchange Act of 1934, as amended (the “Exchange Act”). Based on this
evaluation and on the material weaknesses disclosed in our Annual Report on Form 10-K for the year ended December 31, 2023 which remained
as of September 30, 2024, our principal executive officer and principal financial officer concluded that as of September 30, 2024, our disclosure
controls and procedures were not effective to ensure that information required to be disclosed by us in reports filed or submitted under
the Exchange Act is being recorded, processed, summarized, and reported within the time periods specified in the Securities and Exchange
Commission’s rules and forms, and that our disclosure controls are not effectively designed to ensure that information required
to be disclosed by us in the reports that we file or submit under the Exchange Act is being accumulated and communicated to management,
including our principal executive officer and principal financial officer, or persons performing similar functions, as appropriate to
allow timely decisions regarding required disclosure.
Because
of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Projections of any evaluation
of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that
the degree of compliance with the policies or procedures may deteriorate. All internal control systems, no matter how well designed,
have inherent limitations. Therefore, even those systems determined to be effective can provide only reasonable assurance with respect
to financial statement preparation and presentation.
Changes
in Internal Control over Financial Reporting
While
changes in the Company’s internal control over financial reporting occurred during the quarter ended September 30, 2024, as the Company
began implementation of the remediation steps described in our annual report dated December 31, 2023, we believe that there were no changes
in the Company’s internal control over financial reporting during the quarter ended September 30, 2024, that have materially affected,
or are reasonably likely to materially affect, the Company’s internal control over financial reporting.
PART
II
OTHER
INFORMATION
ITEM
1 - LEGAL PROCEEDINGS
We
are not currently a party to any material legal proceedings. From time to time, we may become involved in legal proceedings arising in
the ordinary course of our business. Regardless of outcome, litigation can have an adverse impact on us due to defense and settlement
costs, diversion of management resources, negative publicity, reputational harm and other factors.
ITEM
1A - RISK FACTORS
Smaller
reporting companies are not required to provide the information required by this item.
ITEM
2 - UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
None.
ITEM
3 - DEFAULTS UPON SENIOR SECURITIES
None.
ITEM
4 - MINE SAFETY DISCLOSURES
Not
applicable.
ITEM
5 - OTHER INFORMATION
None.
ITEM
6 - EXHIBITS
Exhibit
Number |
|
Exhibit
Description |
|
|
|
1.1 |
|
Form of Underwriting Agreement between the Company and Aegis Capital Corp. incorporated by reference to Exhibit 1.1 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
3.1 |
|
Amended and Restated Articles of Incorporation of Impact BioMedical Inc. dated July 29, 2020 incorporated by reference to Exhibit 3.1 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
3.2 |
|
Certificate of Amendment to the Amended and Restated Articles of Incorporation of Impact BioMedical Inc. incorporated by reference to Exhibit 3.2 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
3.3 |
|
Certificate of Amendment to the Amended and Restated Articles of Incorporation of Impact BioMedical Inc. incorporated by reference to Exhibit 3.3 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
3.4 |
|
Certificate of Amendment to the Amended and Restated Articles of Incorporation of Impact BioMedical Inc. incorporated by reference to Exhibit 3.4 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
3.5 |
|
Bylaws of the Company incorporated by reference to Exhibit 3.5 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
3.6 |
|
Certificate of Designation of Series A Convertible Preferred Stock incorporated by reference to Exhibit 3.6 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
4.1 |
|
Form of Underwriter Warrant incorporated by reference to Exhibit 4.1 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.1 |
|
Share Exchange Agreement dated as of April 27, 2020, among Document Security Systems, Inc., DSS BioHealth Security, Inc., Singapore Development Limited and Global BioMedical Pte Ltd. incorporated by reference to Exhibit 10.1 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.2 |
|
Subscription Agreement dated December 19, 2020, between the Company and BioMed Technologies Asia Pacific Holdings Limited incorporated by reference to Exhibit 10.2 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.3 |
|
Promissory Note with Dustin Michael Crum dated February 21, 2021 incorporated by reference to Exhibit 10.3 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.4 |
|
Stock Purchase Agreement dated March 15, 2021 between the Company and Vivacitas Oncology Inc. incorporated by reference to Exhibit 10.4 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.5 |
|
Convertible Promissory Note dated May 14, 2021 incorporated by reference to Exhibit 10.5 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
10.6 |
|
Revolving Promissory Note dated December 31, 2020 incorporated by reference to Exhibit 10.6 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.7 |
|
Royalty Agreement by and between Global BioLife Inc. and Chemia Corporation, dated August 15, 2018 incorporated by reference to Exhibit 10.7 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.8 |
|
Addendum to Royalty Agreement by and between Global BioLife Inc. and Chemia Corporation, dated November 27, 2018 incorporated by reference to Exhibit 10.8 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062 ) filed with the SEC on November 21, 2023. |
|
|
|
10.9 |
|
Distribution Agreement by and between BioMed Technologies Asia Pacific Holdings Limited and Impact BioMedical Inc., dated December 9, 2020 incorporated by reference to Exhibit 10.9 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.10 |
|
Global BioLife, Inc. Stockholders’ Agreement among Global BioLife, Inc., Global BioMedical, Inc., Holista Colltech Limited, and GRDG Sciences, LLC, dated April 26, 2017 incorporated by reference to Exhibit 10.10 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.11 |
|
Amendment No. 1 to Global BioLife, Inc. Stockholders’ Agreement among Global BioLife, Inc., Global BioMedical, Inc., Holista Colltech Limited, and GRDG Sciences, LLC, dated May 22, 2018 incorporated by reference to Exhibit 10.11 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.12 |
|
Amendment No. 2 to Global BioLife, Inc. Stockholders’ Agreement among Global BioLife, Inc., Global BioMedical, Inc., Holista Colltech Limited, and GRDG Sciences, LLC, dated August 2020 incorporated by reference to Exhibit 10.12 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.13 |
|
Impact BioLife Science, Inc. Stockholders Agreement among Impact BioLife Science, Inc., Impact BioMedical Inc. and GRDG Sciences, LLC, dated December 11, 2020 incorporated by reference to Exhibit 10.13 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.14 |
|
Licensing Proceeds Distribution Agreement with GRDG Sciences, LLC dated May 16, 2022 incorporated by reference to Exhibit 10.14 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.15 |
|
Amendment No. 1 to Revolving Promissory Note dated December 31, 2021 incorporated by reference to Exhibit 10.15 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.16 |
|
Amendment No. 2 to Revolving Promissory Note dated March 31, 2022 incorporated by reference to Exhibit 10.16 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.17 |
|
License Agreement with ProPhase Labs, Inc. dated March 17, 2022 incorporated by reference to Exhibit 10.17 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.18 |
|
License Agreement with ProPhase Labs, Inc. dated July 18, 2022 incorporated by reference to Exhibit 10.18 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.19 |
|
Licensing Proceeds Distribution Agreement with GRDG Sciences, LLC dated February 15, 2022 incorporated by reference to Exhibit 10.19 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.20 |
|
Share Exchange Agreement between Impact BioMedical Inc. and DSS BioHealth Security, Inc. incorporated by reference to Exhibit 10.20 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
10.21 |
|
Amendment to Promissory Note effective January 18, 2024 between Impact BioMedical Inc. and DSS, Inc. incorporated by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K (Commission File No. 333-253037) filed with the SEC on January 22, 2024. |
14.1 |
|
Impact BioMedical Employee Handbook incorporated by reference to Exhibit 14.1 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
16.1 |
|
Letter from Turner Stone & Company LLP incorporated by reference to Exhibit 16.1 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
21.1 |
|
List of subsidiaries of Impact BioMedical Inc. incorporated by reference to Exhibit 21.1 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
23.2 |
|
Consent of Grassi & Co., CPAs, P.C. incorporated by reference to Exhibit 23.2 to the Company’s Amendment to the Registration Statement on Form S-1 (No. 333-275062) filed with the SEC on November 21, 2023. |
|
|
|
31.1 |
|
Certification of Principal Executive Officer pursuant to Rules 13a-14(a) and 15d-14(a) of the Securities Exchange Act, as amended. |
|
|
|
31.2 |
|
Certification of Principal Financial Officer pursuant to Rules 13a-14(a) and 15d-14(a) of the Securities Exchange Act, as amended. |
|
|
|
32.1 |
|
Certification of Principal Executive Officer and Principal Financial Officer pursuant to Rules 13a-14(b) or 15d-14(b) of the Securities and Exchange Act, as amended, and 18 U.S.C. Section 1350. |
|
|
|
101.INS |
|
Inline
XBRL Instance Document |
|
|
|
101.SCH |
|
Inline
XBRL Taxonomy Extension Schema Document |
|
|
|
101.CAL |
|
Inline
XBRL Taxonomy Extension Calculation Linkbase Document |
|
|
|
101.DEF |
|
Inline
XBRL Taxonomy Extension Definition Linkbase Document |
|
|
|
101.LAB |
|
Inline
XBRL Taxonomy Extension Label Linkbase Document |
|
|
|
101.PRE |
|
Inline
XBRL Taxonomy Extension Presentation Linkbase Document |
|
|
|
104 |
|
Cover
Page Interactive Data File (embedded within the Inline XBRL document) |
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by
the undersigned thereunto duly authorized.
|
IMPACT
BIOMEDICAL, INC. |
|
|
|
November 12, 2024 |
By:
|
/s/
Frank D. Heuszel |
|
|
Frank
D. Heuszel |
|
|
Chief
Executive Officer |
|
|
(Principal
Executive Officer) |
|
|
|
November 12, 2024 |
By: |
/s/
Todd D. Macko |
|
|
Todd
D. Macko |
|
|
Chief
Financial Officer |
|
|
(Principal Financial and Accounting Officer)
|
Exhibit
31.1
CERTIFICATION
I,
Frank D. Heuszel, certify that:
1. |
I
have reviewed this quarterly report on Form 10-Q of Impact BioMedical Inc., a Nevada corporation (the “registrant”); |
|
|
2. |
Based
on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary
to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to
the period covered by this report; |
|
|
3. |
Based
on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material
respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in
this report; |
|
|
4. |
The
registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures
(as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange
Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
|
(a) |
Designed
such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision,
to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others
within those entities, particularly during the period in which this report is being prepared; |
|
|
|
|
(b) |
Designed
such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our
supervision to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements
for external purposes in accordance with generally accepted accounting principles; |
|
|
|
|
(c) |
Evaluated
the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about
the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; |
|
|
|
|
(d) |
Disclosed
in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s
most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected,
or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and |
5. |
The
registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial
reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing
the equivalent functions): |
|
(a) |
All
significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are
reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information;
and |
|
|
|
|
(b) |
Any
fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s
internal control over financial reporting. |
Date:
November 12, 2024 |
|
|
|
/s/
Frank D. Heuszel |
|
Frank
D. Heuszel |
|
Chief
Executive Officer and Director
(Principal Executive Officer) |
|
Exhibit
31.2
CERTIFICATION
I,
Todd D. Macko certify that:
1. |
I
have reviewed this quarterly report on Form 10-Q of Impact BioMedical, Inc., a Nevada corporation (the “registrant”); |
|
|
2. |
Based
on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary
to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to
the period covered by this report; |
|
|
3. |
Based
on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material
respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in
this report; |
|
|
4. |
The
registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures
(as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange
Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
|
(a) |
Designed
such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision,
to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others
within those entities, particularly during the period in which this report is being prepared; |
|
|
|
|
(b) |
Designed
such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our
supervision to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements
for external purposes in accordance with generally accepted accounting principles; |
|
|
|
|
(c) |
Evaluated
the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about
the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; |
|
|
|
|
(d) |
Disclosed
in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s
most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected,
or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and |
5. |
The
registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial
reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing
the equivalent functions): |
|
(a) |
All
significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are
reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information;
and |
|
|
|
|
(b) |
Any
fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s
internal control over financial reporting. |
Date:
November 12, 2024 |
|
|
|
/s/
Todd D. Macko |
|
Todd
D. Macko |
|
Chief
Financial Officer |
|
(Principal
Financial and Accounting Officer) |
|
Exhibit
32.1
Certification
Pursuant to 18 U.S.C. §1350, as Adopted
Pursuant
to §906 of the Sarbanes-Oxley Act of 2002
Pursuant
to the requirement set forth in Rule 13a-14(b) of the Securities Exchange Act of 1934, as amended, (the “Exchange Act”) and
Section 1350 of Chapter 63 of Title 18 of the United States Code (18 U.S.C. §1350), each of the undersigned hereby certifies in
his capacity as an officer of Impact BioMedical, Inc. (the “Company”), that, to the best of his knowledge:
(1)
the Company’s Quarterly Report on Form 10-Q for the quarterly period ended September 30, 2024, to which this Certification is attached
as Exhibit 32.1 (the “Report”) fully complies with the requirements of Section 13(a) or Section 15(d) of the Exchange Act;
and
(2)
the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations
of the Company.
/s/
Frank D. Heuszel |
|
Frank
D. Heuszel |
|
Chief
Executive Officer and Director |
|
(Principal
Executive Officer) |
|
|
|
Date:
November 12, 2024 |
|
|
|
/s/
Todd D. Macko |
|
Todd
D. Macko |
|
Chief
Financial Officer |
|
(Principal
Financial and Accounting Officer) |
|
|
|
Date:
November 12, 2024 |
|
A
certification furnished pursuant to this Item will not be deemed “filed” for purposes of section 18 of the Exchange Act (15
U.S.C. 78r), or otherwise subject to the liability of that section. Such certification will not be deemed to be incorporated by reference
into any filing under the Securities Act or the Exchange Act, except to the extent that the small business issuer specifically incorporates
it by reference.
v3.24.3
Cover - $ / shares
|
9 Months Ended |
|
Sep. 30, 2024 |
Oct. 25, 2024 |
Cover [Abstract] |
|
|
Document Type |
10-Q
|
|
Amendment Flag |
false
|
|
Document Quarterly Report |
true
|
|
Document Transition Report |
false
|
|
Document Period End Date |
Sep. 30, 2024
|
|
Document Fiscal Period Focus |
Q3
|
|
Document Fiscal Year Focus |
2024
|
|
Current Fiscal Year End Date |
--12-31
|
|
Entity File Number |
333-275062
|
|
Entity Registrant Name |
Impact
BioMedical, INC.
|
|
Entity Central Index Key |
0001834105
|
|
Entity Tax Identification Number |
85-3926944
|
|
Entity Incorporation, State or Country Code |
NV
|
|
Entity Address, Address Line One |
1400 Broadfield Blvd
|
|
Entity Address, Address Line Two |
Suite 130
|
|
Entity Address, City or Town |
Houston
|
|
Entity Address, State or Province |
TX
|
|
Entity Address, Postal Zip Code |
77084
|
|
City Area Code |
(281)
|
|
Local Phone Number |
415-6576
|
|
Entity Current Reporting Status |
Yes
|
|
Entity Interactive Data Current |
Yes
|
|
Entity Filer Category |
Non-accelerated Filer
|
|
Entity Small Business |
true
|
|
Entity Emerging Growth Company |
true
|
|
Elected Not To Use the Extended Transition Period |
false
|
|
Entity Shell Company |
false
|
|
Entity Common Stock, Shares Outstanding |
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11,503,955
|
Entity Listing, Par Value Per Share |
$ 0.001
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v3.24.3
Condensed Consolidated Balance Sheets - USD ($)
|
Sep. 30, 2024 |
Dec. 31, 2023 |
Current assets: |
|
|
Cash and cash equivalents |
$ 2,668,000
|
$ 1,000
|
Accounts receivable, net |
|
128,000
|
Current portion of notes receivable |
142,000
|
203,000
|
Prepaid expenses and other current assets |
365,000
|
|
Total current assets |
3,175,000
|
332,000
|
Property, plant and equipment, net |
282,000
|
287,000
|
Notes receivable |
59,000
|
|
Goodwill |
25,093,000
|
25,093,000
|
Other intangible assets, net |
18,086,000
|
18,921,000
|
Total assets |
46,695,000
|
44,633,000
|
Current liabilities: |
|
|
Accounts payable |
1,001,000
|
832,000
|
Accrued expenses and deferred revenue |
102,000
|
230,000
|
Current portion note payable, related party |
35,000
|
12,074,000
|
Total current liabilities |
1,138,000
|
13,136,000
|
Long-term portion note payable, related party |
7,971,000
|
|
Deferred tax liability, net |
3,235,000
|
3,235,000
|
Total liabilities |
12,344,000
|
16,371,000
|
Commitments and contingencies (Note 11) |
|
|
Stockholders’ equity |
|
|
Preferred stock, $.001 par value; 100,000,000 shares authorized, 60,496,041 shares issued and outstanding (60,496,041 on December 31, 2023); Liquidation value $0.001 per share, $60,000 aggregate. $60,000 on December 31, 2023). |
60,000
|
60,000
|
Common stock, $.001 par value; 4,000,000,000 shares authorized, 11,503,955 shares issued and outstanding (10,000,000 on December 31, 2023) |
11,000
|
10,000
|
Additional paid-in capital |
41,838,000
|
38,113,000
|
Accumulated deficit |
(10,561,000)
|
(12,961,000)
|
Total stockholders’ equity of the Company |
31,348,000
|
25,222,000
|
Non-controlling interest in subsidiaries |
3,003,000
|
3,040,000
|
Total stockholders’ equity |
34,351,000
|
28,262,000
|
Total liabilities and stockholders’ equity |
$ 46,695,000
|
$ 44,633,000
|
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v3.24.3
Condensed Consolidated Balance Sheets (Parenthetical) - USD ($)
|
Sep. 30, 2024 |
Dec. 31, 2023 |
Statement of Financial Position [Abstract] |
|
|
Preferred stock, par value |
$ 0.001
|
$ 0.001
|
Preferred stock, shares authorized |
100,000,000
|
100,000,000
|
Preferred stock, shares issued |
60,496,041
|
60,496,041
|
Preferred stock, shares outstanding |
60,496,041
|
60,496,041
|
Preferred stock, liquidation preference per share |
$ 0.001
|
$ 0.001
|
Preferred stock, liquidation preference value |
$ 60,000
|
$ 60,000
|
Common stock, par value |
$ 0.001
|
$ 0.001
|
Common stock, shares authorized |
4,000,000,000
|
4,000,000,000
|
Common stock, shares issued |
11,503,955
|
10,000,000
|
Common stock, shares outstanding |
11,503,955
|
10,000,000
|
X |
- DefinitionFace amount or stated value per share of common stock.
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v3.24.3
Condensed Consolidated Statements of Operations (Unaudited) - USD ($)
|
3 Months Ended |
9 Months Ended |
Sep. 30, 2024 |
Sep. 30, 2023 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Costs and expenses: |
|
|
|
|
Sales, general and administrative compensation |
$ 132,000
|
$ 101,000
|
$ 424,000
|
$ 182,000
|
Sales and marketing |
461,000
|
17,000
|
487,000
|
44,000
|
Professional Fees |
122,000
|
317,000
|
313,000
|
750,000
|
Research and development |
82,000
|
357,000
|
386,000
|
1,055,000
|
Depreciation and Amortization |
281,000
|
280,000
|
840,000
|
840,000
|
Rent and utilities |
4,000
|
|
14,000
|
|
Other operating expenses |
45,000
|
6,000
|
58,000
|
18,000
|
Total costs and expenses |
1,127,000
|
1,078,000
|
2,522,000
|
2,889,000
|
Operating loss |
(1,127,000)
|
(1,078,000)
|
(2,522,000)
|
(2,889,000)
|
Other income (expense): |
|
|
|
|
Interest income |
3,000
|
3,000
|
10,000
|
10,000
|
Change in fair value of embedded derivative |
5,670,000
|
|
5,670,000
|
|
Other income (expense) |
|
|
|
52,000
|
Interest expense |
(305,000)
|
(102,000)
|
(795,000)
|
(319,000)
|
Income (loss) from operations before income taxes |
4,241,000
|
(1,177,000)
|
2,363,000
|
(3,146,000)
|
Income tax benefit |
|
|
|
|
Net income (loss) |
4,241,000
|
(1,177,000)
|
2,363,000
|
(3,146,000)
|
Loss from operations attributed to noncontrolling interest |
6,000
|
15,000
|
37,000
|
45,000
|
Income (loss) attributable to common stockholders |
$ 4,247,000
|
$ (1,162,000)
|
$ 2,400,000
|
$ (3,101,000)
|
Income (loss) per common share: |
|
|
|
|
Basic |
$ 0.37
|
$ (0.02)
|
$ 0.23
|
$ (0.04)
|
Diluted |
$ 0.06
|
$ (0.02)
|
$ 0.03
|
$ (0.04)
|
Shares used in computing loss per common share: |
|
|
|
|
Basic |
11,503,955
|
70,496,041
|
10,506,394
|
70,496,041
|
Diluted |
71,999,996
|
70,496,041
|
71,002,435
|
70,496,041
|
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v3.24.3
Condensed Consolidated Statements of Stockholder's Equity (Unaudited) - USD ($)
|
Common Stock [Member] |
Preferred Stock [Member] |
Additional Paid-in Capital [Member] |
Retained Earnings [Member] |
Parent [Member] |
Noncontrolling Interest [Member] |
Total |
Balance at Dec. 31, 2022 |
$ 70,000
|
|
$ 38,113,000
|
$ (8,567,000)
|
$ 29,616,000
|
$ 3,111,000
|
$ 32,727,000
|
Balance, shares at Dec. 31, 2022 |
70,496,041
|
|
|
|
|
|
|
Net income (loss) |
|
|
|
(3,101,000)
|
(3,101,000)
|
(45,000)
|
(3,146,000)
|
Balance at Sep. 30, 2023 |
$ 70,000
|
|
38,113,000
|
(11,668,000)
|
26,515,000
|
3,066,000
|
29,581,000
|
Balance, shares at Sep. 30, 2023 |
70,496,041
|
|
|
|
|
|
|
Balance at Dec. 31, 2023 |
$ 10,000
|
$ 60,000
|
38,113,000
|
(12,961,000)
|
25,222,000
|
3,040,000
|
28,262,000
|
Balance, shares at Dec. 31, 2023 |
10,000,000
|
60,496,041
|
|
|
|
|
|
Net income (loss) |
|
|
|
2,400,000
|
2,400,000
|
(37,000)
|
2,363,000
|
Issuance of common stock, net of expenses |
$ 1,000
|
|
3,725,000
|
|
3,726,000
|
|
3,726,000
|
Issuance of common stock, net of expenses, shares |
1,500,000
|
|
|
|
|
|
|
Fractional shares as a result of reverse stock split |
|
|
|
|
|
|
|
Fractional shares as a result of reverse stock split, shares |
3,955
|
|
|
|
|
|
|
Balance at Sep. 30, 2024 |
$ 11,000
|
$ 60,000
|
$ 41,838,000
|
$ (10,561,000)
|
$ 31,348,000
|
$ 3,003,000
|
$ 34,351,000
|
Balance, shares at Sep. 30, 2024 |
11,503,955
|
60,496,041
|
|
|
|
|
|
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v3.24.3
Condensed Consolidated Statements of Cash Flows (Unaudited) - USD ($)
|
9 Months Ended |
Sep. 30, 2024 |
Sep. 30, 2023 |
Cash flows from operating activities: |
|
|
Income (loss) from operations |
$ 2,363,000
|
$ (3,146,000)
|
Adjustments to reconcile loss from continuing operations to net cash used by operating activities: |
|
|
Depreciation and amortization |
840,000
|
840,000
|
Change in fair value of embedded derivative |
(5,670,000)
|
|
Decrease (increase) in assets: |
|
|
Accounts receivable |
128,000
|
|
Prepaid expenses and other current assets |
(365,000)
|
8,000
|
Increase (decrease) in liabilities: |
|
|
Accounts payable |
169,000
|
(63,000)
|
Accrued expenses |
(128,000)
|
(57,000)
|
Net cash used by operating activities |
(2,663,000)
|
(2,418,000)
|
Cash flows from investing activities: |
|
|
Purchase of property, plant and equipment |
|
(18,000)
|
Payments received on notes receivable |
2,000
|
2,000
|
Net cash provided (used) by investing activities |
2,000
|
(16,000)
|
Cash flows from financing activities: |
|
|
Borrowings from revolving lines of credit, net |
1,602,000
|
2,633,000
|
Issuances of common stock, net of issuance costs |
3,726,000
|
|
Net cash provided by financing activities |
5,328,000
|
2,633,000
|
Net increase in cash |
2,667,000
|
199,000
|
Cash and cash equivalents at beginning of period |
1,000
|
2,000
|
Cash and cash equivalents at end of period |
$ 2,668,000
|
$ 201,000
|
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v3.24.3
Nature of Operations and Basis of Presentation
|
9 Months Ended |
Sep. 30, 2024 |
Organization, Consolidation and Presentation of Financial Statements [Abstract] |
|
Nature of Operations and Basis of Presentation |
Note
1. Nature of Operations and Basis of Presentation
Nature
of Operations
Impact
BioMedical, Inc., incorporated in the State of Nevada
on October
16, 2018 (the “Company”, “Impact
BioMedical”, “We”, “IBO”), discovers, confirms, and patents unique science and technologies which
can be developed into new offerings in human healthcare and wellness in collaboration with external partners through licensing, co-development,
joint ventures, and other relationships. By leveraging technology and new science with strategic partnerships, we pursue advances
in biopharmaceuticals and over the counter direct to consumer wellness offerings. In addition to existing efforts, we continually
search for and evaluate other potential new offerings to add to our portfolio. Our business model includes partnering and potentially
direct sales for commercialization and distribution. Potential licensors and development partners include pharmaceutical, consumer goods
and services companies and others, who would commercialize IBO technologies in exchange for milestone, and royalty licensing payments.
Impact
has several unique and proprietary technologies that are in continuing development:
Linebacker™
Linebacker is a platform of
small molecule electrophilically enhanced polyphenol compounds with potential application in oncology (solid tumors), inflammatory disorders,
and neurology. Polyphenols are substances found in many nuts, vegetables, and berries. Linebacker compounds are modified Myricetin,
which is a common plant-derived flavonoid. Myricetin exhibits a wide range of activities that include strong antioxidants and anti-inflammatory
activities (source: NIH). Linebacker can potentially be developed as monotherapy or co-therapy to down-regulate PIM (proviral integration
site for Moloney murine leukemia virus) kinase which plays a key role as an oncogene in various cancers (e.g., colon, lung, prostate,
breast). Additional potential applications include inflammatory disorders and neurology. Linebacker-1 and Linebacker-2 compounds
have been licensed to ProPhase Laboratories (NASDAQ: PRPH) for development and potential commercialization worldwide, from which Impact
Biomedical could receive future milestone and royalty payments. Composition and method patents are issued to the company for Linebacker
in the U.S. and other countries.
Laetose™
Laetose technology is derived
from a unique combination of multiple sugars independently with myo-inositol, which demonstrates compelling potential in 1) reducing glycemic
index and caloric intake in foods, 2) application as a therapeutic which inhibits tumor necrosis factor alpha (TNF-α), a cytokine
associated with inflammatory chronic diseases, and 3) a method of reducing or limiting the occurrence of diabetes. The sugar can
be one or a combination of sugars: sucrose, fructose, isoglucose, and galactose. Laetose has a unique composition patent allowed in the
United States and patents are pending in other countries worldwide. IBO is actively seeking potential partners for further development
and commercialization of Laetose as a consumer packaged or biopharmaceutical offering worldwide.
Functional
Fragrance Formulation (“3F”)
3F is a suite of organic “functional
fragrances” containing specialized botanical ingredients (e.g., terpenes) with potential application as an antimicrobial, or as
an additive in insect repellents, detergents, lotions, shampoo, fabrics, and other substances to increase effectiveness. IBO has
partnered with the Chemia Corporation (St. Louis, MO) to pursue development of the 3F technology. Chemia is a leading developer and manufacturer
of fragrances and flavors. Composition patents have issued in the U.S. and are pending in other countries. In addition to Chemia,
IBO is actively seeking potential partners for the further development and commercialization of 3F worldwide, given the broad application
of this technology.
Equivir™/Equivir
G
Equivir technology is a novel
blend of FDA Generally Recognized as Safe (GRAS) eligible polyphenols (e.g., Myricetin, Hesperetin, Piperine) which have demonstrated
antiviral effects with additional potential applications such as health supplements or medication. Polyphenols are substances found in
many nuts, vegetables, and berries. Myricetin is a member of the flavonoid class of polyphenolic compounds with antioxidant properties.
Hesperitin is a flavanone and Piperine is an alkaloid, commonly found in black pepper. Equivir/Equivir G is licensed to ProPhase
Laboratories for development and commercialization worldwide. ProPhase Lab’s initial focus is for potential use as an over-the-counter
health supplement offering for upper respiratory wellness. Additional applications could be pursued in the future. Method and composition
patents are issued in the U.S. and other countries.
Emerging
Technology
IBO
continually evaluates additional technologies that are in various phases of development which can be advanced to patent filings and allowances.
These include, and are not limited to biopharmaceuticals, indoor air quality products, preservatives, bioplastics, personalized medicine
(e.g., genomics, diagnostics), nanotechnology, cannabis products and technology, pain management, and others. These activities
include discussions with inventors, scientists, universities, research foundations, and other parties, which, subject to completion
of diligence, and approval of the respective management, could potentially expand the offerings of IBO.
As
of the date of this report, we have not generated significant revenues from operations. We cannot guarantee we will be successful in
our business operations. Our business is subject to risks inherent in the establishment of a new business enterprise, including possible
delays in our research, testing and marketing efforts or wider economic downturns.
|
X |
- DefinitionThe entire disclosure for the nature of an entity's business, major products or services, principal markets including location, and the relative importance of its operations in each business and the basis for the determination, including but not limited to, assets, revenues, or earnings. For an entity that has not commenced principal operations, disclosures about the risks and uncertainties related to the activities in which the entity is currently engaged and an understanding of what those activities are being directed toward.
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v3.24.3
Summary of Significant Accounting and Reporting Policies
|
9 Months Ended |
Sep. 30, 2024 |
Accounting Policies [Abstract] |
|
Summary of Significant Accounting and Reporting Policies |
Note
2. Summary of Significant Accounting and Reporting Policies
Basis
of Presentation and Principles of Consolidation
The
Company’s consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the
United States of America (“U.S. GAAP”). The consolidated financial statements include all accounts of the Company and its
majority owned and controlled subsidiaries. The Company consolidates entities in which it owns more than 50% of the voting common stock
and controls operations. All intercompany transactions and balances among consolidated subsidiaries have been eliminated. Non–controlling
interest represents the minority equity investment in the Company’s subsidiaries, plus the minority investors’ share of the
net operating results and other components of equity relating to the non–controlling interest.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
The
consolidated financial statements include all accounts of the entities as of the reporting period ending dates and for the reporting
periods as follows:
Schedule
of Condensed Financial Statements
Name of consolidated
subsidiary | |
State or other
jurisdiction of
incorporation or
organization | |
Date of incorporation
or formation | |
Attributable
interest as of
September 30, 2024 | | |
Attributable
interest as of
December 31, 2023 | |
| |
| |
| |
| | |
| |
Global BioMedical, Inc. | |
Nevada | |
April 18, 2017 | |
| 90.9 | % | |
| 90.9 | % |
Global BioLife, Inc. | |
Nevada | |
April 14, 2017 | |
| 81.8 | % | |
| 81.8 | % |
BioLife Sugar, Inc | |
Nevada | |
April 23, 2018 | |
| 90.9 | % | |
| 90.9 | % |
Happy Sugar Inc | |
Nevada | |
August 17, 2018 | |
| 81.8 | % | |
| 81.8 | % |
Sweet Sense Inc. | |
Nevada | |
April 30, 2018 | |
| 95.5 | % | |
| 95.5 | % |
Global Sugar Solutions Inc. | |
Nevada | |
November 7, 2019 | |
| 100 | % | |
| 100 | % |
As
of September 30, 2024, and December 31, 2023, the aggregate noncontrolling interest was equity of $3,003,000 and $3,040,000,
respectively, which are separately disclosed on the Consolidated Balance Sheets.
Use
of estimates
The
preparation of consolidated financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that
affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities as of the dates of the balance
sheets and reported amounts of revenues and expenses during the reporting periods. Actual results could differ from these estimates.
Reclassifications
Costs
associate with Sales and marketing have been reclassed from Other operating expenses for the three and nine months ended September 30,
2023 to conform with current period presentation. Also, cost associated with Professional fees for the three and nine months ended September 30, 2023 and the nine
months September 30, 2024 have been reclassified to Research and development to conform with current period presentation.
Loss
per Share
Basic
loss per share is computed by dividing the net loss attributable to the common stockholders by weighted average number of shares of common
stock outstanding during the period. Fully diluted loss per share is computed like basic loss per share except that the denominator is
increased to include the number of additional common shares that would have been outstanding if the potential common shares had been
issued and if the additional common shares were dilutive. There were no dilutive financial instruments issued or outstanding for the
three and nine months ended September 30, 2023. For the three and nine months ending September 30, 2024, there are 60,496,041 shares of Series A Convertible Preferred
Shares which are not eligible for conversion until April 10, 2027.
Fair
Value of Financial Instruments
Fair
value is defined as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between
market participants at the measurement date. The Fair Value Measurement Topic of the Financial Accounting Standards Board (“FASB”)
Accounting Standards Codification (“ASC”) establishes a three-tier fair value hierarchy which prioritizes the inputs used
in measuring fair value. The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical assets
or liabilities (Level 1 measurements) and the lowest priority to unobservable inputs (Level 3 measurements). These tiers include:
●
Level 1, defined as observable inputs such as quoted prices for identical instruments in active markets,
●
Level 2, defined as inputs other than quoted prices in active markets that are either directly or indirectly observable such as quoted
prices for similar instruments in active markets or quoted prices for identical or similar instruments in markets that are not active;
and
●
Level 3, defined as unobservable inputs in which little or no market data exists, therefore requiring an entity to develop its own assumptions,
such as valuations derived from valuation techniques in which one or more significant inputs or significant value drivers are unobservable.
The
carrying amounts reported in the balance sheet of cash and cash equivalents, prepaids, accounts payable and accrued expenses approximate
fair value because of the immediate or short-term maturity of these financial instruments. The fair value of notes receivable approximates
their carrying value as the stated or discounted rates of the notes do reflect recent market conditions. The Company’s investments
are recorded at cost as the fair value of these investment in is not readily available. The fair value of notes payable approximates
its carrying value as the stated interest rate reflects recent market conditions.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Cash
and cash equivalents
The
Company considers all highly liquid investments with a maturity of three months or less at the date of acquisition to be cash equivalents.
There were no cash equivalents as of September 30, 2024 and December 31, 2023.
Notes
receivable, unearned interest, and related recognition
The
Company records all future payments of principal and interest on notes as notes receivable, which are then offset by the amount of any
related unearned interest income. For financial statement purposes, the Company reports the net investment in the notes receivable on
the consolidated balance sheet as current or long-term based on the maturity date of the underlying notes. Such net investment is comprised
of the amount advanced on the loans, adjusting for net deferred loan fees or costs incurred at origination, amounts allocated to warrants
received upon origination, and any payments received in advance, if applicable. The unearned interest is recognized over the term of
the notes and the income portion of each note payment is calculated so as to generate a constant rate of return on the net balance outstanding.
If applicable, any net deferred loan fees or costs, together with discounts recognized in connection with warrants acquired at origination,
are accreted as an adjustment to yield over the term of the loan. (Note 3)
Goodwill
Goodwill
is the excess of cost of an acquired entity over the fair value of amounts assigned to assets acquired and liabilities assumed in a business
combination. Goodwill is subject to impairment testing at least annually and will be tested for impairment between annual tests, which
will take place during the fourth quarter in 2024, if an event occurs or circumstances change that would indicate the carrying amount
may be impaired. FASB ASC Topic 350 provides an entity with the option to first assess qualitative factors to determine whether the existence
of events or circumstances leads to a determination that it is more likely than not that the fair value of a reporting unit is less than
its carrying amount. Some of the qualitative factors considered in applying this test include consideration of macroeconomic conditions,
industry and market conditions, cost factors affecting the business, and overall financial performance of the business. If, after completing
the assessment, it is determined that it is more likely than not that the fair value of a reporting unit is less than its carrying value,
the Company will proceed to a quantitative test. If qualitative factors are not deemed sufficient to conclude that the fair value of
the reporting unit more likely than not exceeds its carrying value, then a one-step approach is applied in making an evaluation. The
evaluation utilizes an income approach (discounted cash flow analysis). The computations require management to make significant estimates
and assumptions, including, among other things, selection of comparable publicly traded companies, the discount rate applied to future
earnings reflecting a weighted average cost of capital, and earnings growth assumptions. The Company believes the estimates and assumptions
used in our impairment assessments are reasonable and based on available market information, but variations in any of the assumptions
could result in materially different calculations of fair value and determinations of whether or not an impairment is indicated. A discounted
cash flow analysis requires management to make various assumptions about future sales, operating margins, capital expenditures, working
capital, and growth rates. Cash flow projections are derived from one-year budgeted amounts plus an estimate of later period cash flows,
all of which are determined by management. Subsequent period cash flows are developed for each reporting unit using growth rates that
management believes are reasonably likely to occur. Impairment of goodwill is measured as the excess of the carrying amount of goodwill
over the fair values of recognized and unrecognized assets and liabilities of the reporting unit. No impairment was recognized during
the three or nine months ended September 30, 2024 and 2023. (Note 5)
Intangible
Assets
The
estimated fair values of acquired intangibles are generally determined based upon future economic benefits such as earnings and cash
flows. Acquired identifiable intangible assets are recorded at fair value and are amortized over their estimated useful lives. Acquired
intangible assets with an indefinite life are not amortized but are reviewed for impairment at least annually as of December 31st,
or more frequently whenever events or changes in circumstances indicate that the carrying amounts of those assets are below their estimated
fair values. Impairment is tested under ASC 350. No impairment was recognized for the three or nine months ended September 30, 2024,
and 2023. (Note 6)
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Recoverability
of Long-Lived Assets
We
evaluate long-lived assets such as property, equipment and definite lived intangible assets, such as patents, for impairment whenever
events or circumstances indicate that the carrying value of the assets recognized in our financial statements may not be recoverable.
Factors that we consider include whether there has been a significant decrease in the market value of an asset, a significant change
in the way an asset is being utilized, or a significant change, delay or departure in our strategy for that asset, or a significant change
in the macroeconomic environment. Our assessment of the recoverability of long-lived assets involves significant judgment and estimation.
These assessments reflect our assumptions, which, we believe, are consistent with the assumptions hypothetical marketplace participants
use. Factors that we must estimate when performing recoverability and impairment tests include, among others, forecasted revenue, margin
costs and the economic life of the asset. If impairment is indicated, we determine if the total estimated future cash flows on an undiscounted
basis are less than the carrying amounts of the asset or assets. If so, an impairment loss is measured and recognized.
Our
impairment loss calculations require that we apply judgment in identifying asset groups, estimating future cash flows, determining asset
fair values, and estimating asset’s useful lives. The Company reviews identifiable amortizable intangible assets for impairment
whenever events or changes in circumstances indicate that the carrying value of the assets may not be recoverable. Determination of recoverability
is based on the lowest level of identifiable estimated undiscounted cash flows resulting from use of the asset and its eventual disposition.
Measurement of any impairment loss is based on the excess of the carrying value of the asset over its fair value. Based on the uncertainty
of forecasts inherent with a new product, events such as the failure to generate forecasted revenue from new products could result in
a non-cash impairment in future periods.
Derivative Accounting
The Company analyzes all financial instruments with
features of both liabilities and equity under ASC 480, “Distinguishing Liabilities from Equity” and ASC 815, “Derivatives
and Hedging”. Derivative liabilities are adjusted to reflect fair value at each period end, with any increase or decrease
in the fair value being recorded in results of operations as adjustments to fair value of derivatives. The effects of interactions between
embedded derivatives are calculated and accounted for in arriving at the overall fair value of the financial instruments. Also, the fair
value of freestanding derivative instruments such as warrant and option derivatives are valued using the Black-Scholes simulation
model. The Company has determined that Note payable, related party contains an embedded derivative in the form of payment via equity and
has accounted for it in accordance with ASC 815. (see Note 7).
Revenue
Recognition
The
Company has adopted ASC Topic 606, Revenue from Contracts with Customers (“Topic 606”). The Company enters
into licensing and development agreements with collaborators for the development of its technologies. The terms of these agreements contain
multiple performance obligations which may include (i) licenses, or options to obtain licenses, to the Company’s technology, (ii)
rights to future technological improvements, and/or (iii) research activities to be performed on behalf of the collaborative partner.
Payments to the Company under these agreements may include upfront fees, option fees, exercise fees, payments based upon the achievement
of certain milestones, and royalties on product sales. Revenue is recognized when a customer obtains control of promised goods or services,
in an amount that reflects the consideration which the entity expects to receive in exchange for those goods or services. In determining
the appropriate amount of revenue to be recognized as it fulfills its obligations under the agreements, the Company performs the following
steps: (i) identification of the promised goods or services in the contract; (ii) determination of whether the promised goods or services
are performance obligations including whether they are distinct in the context of the contract; (iii) measurement of the transaction
price, including the constraint on variable consideration; (iv) allocation of the transaction price to the performance obligations; and
(v) recognition of revenue when or as the Company satisfies each performance obligation.
The
Company only applies the five-step model to contracts when it is probable that the Company will collect the consideration to which it
is entitled in exchange for the goods or services it transfers to the customer. At contract inception, once the contract is determined
to be within the scope of ASC 606, the Company assesses the goods or services promised within each contract and determines those that
are performance obligations and assesses whether each promised good or service is distinct. The Company then recognizes as revenue the
amount of the transaction price that is allocated to the respective performance obligation when or as the performance obligation is satisfied.
Research
and Development
Research
and development costs are expensed as incurred. Total research and development costs were $386,000 for the nine months ended September
30, 2024, and $1,055,000 for nine months ended September 30, 2023.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
Provision
for Credit Losses
On
January 1, 2022, the Company adopted amended accounting guidance “ASU No.2016-13 – Credit Losses” which requires
an allowance for credit losses to be deducted from the amortized cost basis of financial assets to present the net carrying value at
the amount that is expected to be collected over the contractual term of the asset considering relevant information about past events,
current conditions, and reasonable and supportable forecasts that affect the collectability of the reported amount. In estimating expected
losses in the loan and lease portfolio, borrower-specific financial data and macro-economic assumptions are utilized to project losses
over a reasonable and supportable forecast period. Assumptions and judgment are applied to measure amounts and timing of expected future
cash flows, collateral values and other factors used to determine the borrowers’ abilities to repay obligations. After the forecast
period, the Company utilizes longer-term historical loss experience to estimate losses over the remaining contractual life of the loans.
Prior to 2022, the allowance for credit losses represented the amount that in management’s judgment reflected incurred credit losses
inherent in the loan and lease portfolio as of the balance sheet date. As of September 30, 2024 and December 31, 2023 the Company has
deemed that no reserve on credit losses were necessary.
Continuing
Operations and Going Concern
The
accompanying consolidated financial statements have been prepared assuming that the Company will continue as a going concern. This basis
of accounting contemplates the recovery of our assets and the satisfaction of liabilities in the normal course of business. As reflected
in the accompanying financial statements the Company has incurred operating losses as well as negative cash flows from operating and
investing activities over the past two years. These factors raise substantial doubt about the Company’s ability to continue as
a going concern within one year of the date that the financial statements are issued. These consolidated financial statements do not
include any adjustments to the specific amounts and classifications of assets and liabilities, which might be necessary should we be
unable to continue as a going concern.
To
continue as a going concern, the Company completed an initial public offering on September 16, 2024 raising $3,726,000
net of issuance costs and is currently listed on the NYSE American under the ticker symbol IBIO. The Company’s management
intends to take additional actions necessary to continue as a going concern. Management’s plans concerning these matters include,
among other things, monetization of its intellectual properties, and tightly controlling operating costs.
Recent
Accounting Standards
The
Financial Accounting Standards Board (FASB) issues various Accounting Standards Updates relating to the treatment and recording of certain
accounting transactions. There are several new accounting pronouncements issued by FASB which are not yet effective. Each of these pronouncements,
as applicable, has been or will be adopted by the Company. As of September 30, 2024, none of these pronouncements are expected to have
a material effect on the financial position, results of operations or cash flows of the Company.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
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v3.24.3
Notes Receivable
|
9 Months Ended |
Sep. 30, 2024 |
Receivables [Abstract] |
|
Notes Receivable |
Note
3. Notes Receivable
On
February 19, 2021, Impact BioMedical, Inc, entered into a promissory note with an individual. The Company loaned the principal sum of
$206,000, with interest at a rate of 6.5%, and maturity date of August 19, 2022 later amended to February 19, 2026. Monthly payments
are due on the twenty-first day of each month and continuing each month thereafter until February 19, 2026. This note is secured by certain
real property situated in Collier County, Florida. The outstanding principal and interest as of September 30, 2024 and December 31, 2023,
was approximately $201,000 and $203,000, respectively. At September 30, 2024, $142,000 is classified in Current notes receivable and
the remaining $59,000 is classified as Notes receivable on the accompanying consolidated balance sheets. At December 31, 2023, $203,000
is classified in Current notes receivable.
|
X |
- DefinitionThe entire disclosure for claims held for amounts due to entity, excluding financing receivables. Examples include, but are not limited to, trade accounts receivables, notes receivables, loans receivables. Includes disclosure for allowance for credit losses.
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v3.24.3
Property, Plant and Equipment, Net
|
9 Months Ended |
Sep. 30, 2024 |
Property, Plant and Equipment [Abstract] |
|
Property, Plant and Equipment, Net |
Note
4. Property, Plant and Equipment, Net
Property,
plant and equipment consisted of the following as of:
Schedule
of Property Plant and Equipment
| |
Estimated | |
September 30, | | |
December 31, | |
| |
Useful Life | |
2024 | | |
2023 | |
Machinery and equipment | |
5-10 years | |
$ | 30,000 | | |
$ | 30,000 | |
Construction in progress | |
| |
| 263,000 | | |
| 263,000 | |
Total Cost | |
| |
| 293,000 | | |
| 293,000 | |
Less accumulated depreciation | |
| |
| 11,000 | | |
| 6,000 | |
Property, plant and equipment, net | |
| |
$ | 282,000 | | |
$ | 287,000 | |
Depreciation
expense for the nine months ended September 30, 2024 and 2023 was approximately $5,000 and $4,000, respectively.
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- DefinitionThe entire disclosure for long-lived, physical asset used in normal conduct of business and not intended for resale. Includes, but is not limited to, work of art, historical treasure, and similar asset classified as collections.
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v3.24.3
Goodwill
|
9 Months Ended |
Sep. 30, 2024 |
Goodwill and Intangible Assets Disclosure [Abstract] |
|
Goodwill |
Note
5. Goodwill
Goodwill
balances and activity for the nine months ended September 30, 2024 and year ended December 31, 2023 consisted of the following:
Schedule
of Goodwill
| |
| | |
Balance at December 31, 2023 | |
$ | 25,093,000 | |
Goodwill adjustment | |
| - | |
Balance at September 30, 2024 | |
$ | 25,093,000 | |
As
of September 30, 2023, management performed annual goodwill impairment testing. No goodwill impairment was identified as a result of
these tests. As of September 30, 2023, a quantitative analysis was prepared utilizing the Market Approach and Income Approach valuing
the Company. The guideline public company Market Approach produced a mean business enterprise value indication using estimated 2026 results
of $49.8 million. The Income Approach was based upon the use of a discounted pro forma cash flow model and produced a business enterprise
value indication of $44.9 million. A weighting of 30% to the weighted value indicated was applied under the Market Approach, and a weighting
of 70% to the value indicated under the Income Approach. A lower weighting was applied to the Market Approach due to the fact of using
forecasted earnings of the Company. Based upon the above weightings, an initial value of $46.4 million for Impact was calculated. Adding
cash of $201,000 to the initial business enterprise value produced a concluded business enterprise value of $46.6 million (rounded) for
Impact. Subtracting interest-bearing debt of $11.9 million, results in a Fair Value for the common equity of Impact of $34.7 million.
As of September 30, 2023, the indicated equity value exceeded the carrying amount by approximately $5.1 million or 14.7%. No circumstances
or events have occurred since the most recent analysis that would indicate the need for an impairment.
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v3.24.3
Intangible Assets
|
9 Months Ended |
Sep. 30, 2024 |
Goodwill and Intangible Assets Disclosure [Abstract] |
|
Intangible Assets |
Note
6. Intangible Assets
The
definite-lived intangible assets, to be amortized over 20 years, balances, and activity for the nine months ended September 30, 2024
and year ended December 31, 2023 consisted of the following:
Schedule
of Intangible Assets
| |
September 30, 2024 | | |
December 31, 2023 | |
| |
Gross
Carrying Amount | | |
Accumulated Amortization | | |
Net
Carrying Amount | | |
Gross
Carrying Amount | | |
Accumulated Amortization | | |
Net
Carrying Amount | |
Definitive-lived: | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Developed technology | |
$ | 22,260,000 | | |
$ | (4,174,000 | ) | |
$ | 18,086,000 | | |
$ | 22,260,000 | | |
$ | (3,339,000 | ) | |
$ | 18,921,000 | |
Total | |
$ | 22,260,000 | | |
$ | (4,174,000 | ) | |
$ | 18,086,000 | | |
$ | 22,260,000 | | |
$ | (3,339,000 | ) | |
$ | 18,921,000 | |
Amortization
expense for the nine months ended September 30, 2024 and 2023 was approximately $835,000 and $835,000, respectively.
The
following table represents future amortization of developed technologies for the years ending December 31:
Schedule
of Future Amortization of Developed Technologies
| |
| | |
2024 | |
$ | 279,000 | |
2025 | |
$ | 1,113,000 | |
2026 | |
$ | 1,113,000 | |
2027 | |
$ | 1,113,000 | |
2028 | |
$ | 1,113,000 | |
Thereafter | |
$ | 13,355,000 | |
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
|
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v3.24.3
Note payable, related party
|
9 Months Ended |
Sep. 30, 2024 |
Debt Disclosure [Abstract] |
|
Note payable, related party |
Note
7. Note payable, related party
On
December 31, 2020, and later amended, the Company executed a Revolving Promissory Note (“Note”) with DSS, a related
party, which accrues interest at a rate of 4.25%
and is due in full at the maturity date of September
30, 2030. The Note was further amended on July 24, 2024 with an effective date of September 16, 2024 to i) allow the Company
to pay certain principal and/or interest payments owing under the repayment terms in an exchange for potential of equity in the
Company, ii) change the quarterly interest due dates to the last day of each calendar quarter (i.e. December 31, March 31, June 30
and September 30), iii) to adjust the On Demand feature so that it starts after the 24th month, iv) continue the planned repayment program commencing on the 37th month and
on the last day of each month thereafter through August 31, 2030 to pay a fixed monthly payment of $126,381,
v) to continue the scheduled maturity date of September 30, 2030, and vi) adjusts the interest rate to be the WSJ Prime Rate plus 0.50%.
As of September 30, 2024 and December 31, 2023 the outstanding balance, inclusive of interest was $8,006,000
(net of change in fair value of embedded derivative of $5,670,000)
and $12,074,000, respectively. Of
the $8,006,000,
$35,000
is included in Current portion of note payable, related party and the remaining $7,971,000
is included in Long-term portion of note payable, related party at September 30, 2024. The $12,074,000
at December 31, 2023 is included in Current portion of note payable, related party.
A
summary of scheduled principal payments of long-term debt (exclusive of the embedded derivative of $5,670,000), subsequent to September 30,
2024, are as follows:
Schedule
of Principal Payments of Long-term Debt
Year | | |
Amount | |
| 2024 | | |
$ | 35,000 | |
| 2025 | | |
| 781,000 | |
| 2026 | | |
| 12,860,000 | |
The
movement in the liability and derivative components of the Note payable, related party as of December 31,2023 and September 30, 2024
are set out below:
Schedule of Movement of Liability and
Derivative Components of Note Payable
| |
Liability Component | | |
Derivative Component | | |
Total | |
December 31, 2023 | |
$ | 12,074,000 | | |
$ | - | | |
$ | 12,074,000 | |
Change in fair value of embedded derivative | |
| (7,098,000 | ) | |
| 1,428,000 | | |
| (5,670,000 | ) |
Advances on note | |
| 807,000 | | |
| - | | |
| 807,000 | |
Interest expense | |
| 795,000 | | |
| - | | |
| 795,000 | |
September 30, 2024 | |
$ | 6,578,000 | | |
$ | 1,428,000 | | |
$ | 8,006,000 | |
We
considered various valuation methodologies in our analysis of the embedded derivative. Valuation methodologies can generally be aggregated
into the following three approaches: the Market Approach, the Income Approach, and the Cost Approach. Based on our analysis of the facts
and circumstances, in estimating the fair value of the Note payable, related party, we utilized a discounted cash flow method (income
approach), in the form of a Monte Carlo simulation of the Company’s stock price and volume weighted average price (“VWAP”)
throughout 36-month period from the Effective Date relative to its closing stock price and VWAP as of the Valuation Date, or $2.00 and
$2.38, respectively. The simulated analysis estimates the expected note cash flow from the date the first payment is due and until the
equity conversion rights expire under the terms of the Note payable, related party based on the following steps:
1) | Developed
the Note Payable repayment schedule |
2) | Developed
the following inputs underlying the simulation analysis |
3) | Inputs
(i) and (ii), were assigned a normal probability distribution, which has a mean of 0 and
a standard deviation of 1, and a correlation of .9885 based on analysis of the guideline
public companies |
4) | Ran
a simulation with 25,000 trials for purposes of capturing the key inputs discussed above
(i.e., forecasting the stock price and VWAP). |
5) | For
the period from the 37th payment to maturity date, the DCF Method includes the remaining
payments required to be made in cash. |
6) | Captured
the results of the simulation and concluded based on the simulation results |
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v3.24.3
Financial Instruments
|
9 Months Ended |
Sep. 30, 2024 |
Investments, All Other Investments [Abstract] |
|
Financial Instruments |
Note 8. Financial Instruments
Cash, Note payable, related party
The following tables show the Company’s cash,
cash equivalents, restricted cash, and note payable, related party by significant investment category as of:
Schedule of Cash,
Cash Equivalents, Restricted Cash, and Note Payable Related Party by Significant Investment Category
| |
September 30, 2024 |
|
| |
Adjusted
cost | | |
Unrealized Gain/(Loss) | | |
Fair Value | | |
Cash and Cash Equivalents | |
|
Note
Payable,
Related Party |
|
Cash | |
$ | 2,668,000 | | |
$ | - | | |
$ | 2,668,000 | | |
$ | 2,668,000 | |
|
$ |
- |
|
Level 2 | |
| | | |
| | | |
| | | |
| | |
|
|
|
|
Note payble, related party | |
| 13,676,000 | | |
| (5,670,000 | ) | |
| 8,006,000 | | |
| - | |
|
|
8,006,000 |
|
Total | |
$ | 16,344,000 | | |
$ | (5,670,000 | ) | |
$ | 10,674,000 | | |
$ | 2,668,000 | |
|
$ |
8,006,000 |
|
| |
September 30, 2023 | |
| |
Adjusted Cost | | |
Unrealized Gain/(Loss) | | |
Fair Value | | |
Cash and Cash Equivalents | |
Cash | |
$ | 1,000 | | |
$ | - | | |
$ | 1,000 | | |
$ | 1,000 | |
Total | |
$ | 1,000 | | |
$ | - | | |
$ | 1,000 | | |
$ | 1,000 | |
|
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v3.24.3
Stockholders’ Equity
|
9 Months Ended |
Sep. 30, 2024 |
Equity [Abstract] |
|
Stockholders’ Equity |
Note
9. Stockholders’ Equity
On
May 10, 2023, the Company’s Board of Directors approved an amendment to the Articles of Incorporation of the Company to increase
the total number of shares of Common Stock to 4,000,000,000
shares with a par value of $0.001.
Each
share of Common Stock when issued, shall have one (1) vote on all matters presented to the stockholders. Our
Amended and Restated Articles of Incorporation also authorized 100,000,000
shares of preferred stock, par value $0.001
per share. On May 11, 2023, the Company effected
a forward split. As a result, there were 3,877,282,251
shares of our Common Stock and no
shares of preferred stock issued and outstanding.
Prior to the split, there were 125,073,621
shares of our Common Stock and no
shares of preferred stock issued and outstanding.
On October 31, 2023, the Company effected a reverse stock split of 1 for 55. Also on October 31, 2023, DSS BioHealth
Securities, Inc., the Company’s largest shareholder converted 60,496,041
shares of Common Stock into 60,496,041
shares of Series
A Convertible Preferred Shares, reducing its ownership of the Company’s Common Stock from approximately 88% to approximately 12%.
As of December 31, 2023, there were 10,000,000
shares of our Common Stock and 60,496,041
shares
of preferred stock issued and outstanding.
On
August 8, 2023 DSS, the Company’s largest shareholder, distributed to its shareholders of record on July 10, 2023 4 shares of Impact
Bio’s stock for 1 share they owned. Each share of Impact BioMedical distributed as part of the distribution will not be eligible
for resale until 180 days from the date Impact BioMedical’s initial public offering becomes effective under the Securities Act,
subject to the discretion of the Company to lift the restriction sooner.
On
October 31, 2023, the Company effected a reverse stock split of 1 for 55. As of December 31, 2023, and December 31, 2022, there were 3,877,282,251
shares of our Common Stock issued and outstanding which was converted to 70,496,041
shares. Also on October 31, 2023, DSS BioHealth Securities, Inc., the Company’s largest shareholder converted 60,496,041
shares of Common Stock into 60,496,041
shares of Series A Convertible Preferred
Shares, reducing its ownership of the Company’s Common Stock from approximately 88% to approximately 12%. The Series A
Convertible Preferred Shares are not eligible for conversion until April 10, 2027.
On
September 16, 2024, Impact Biomedical Inc., entered into an underwriting agreement (the “Underwriting Agreement”) with
Revere Securities, LLC., as representative (the “Representative”) of the underwriters named therein (the
“Underwriters”), pursuant to which the Company agreed to sell to the Underwriters in a firm commitment initial public
offering (the “Offering”) an aggregate of 1,500,000
of the Company’s shares of common stock, par value $0.001
per share at a public offering price of $3.00
per share. On September 17, 2024, the Company closed the Offering, and as of September 30, 2024 there were 11,503,955
shares of common stock issued and outstanding. The total net proceeds to the Company from the Offering, after deducting discounts,
expenses allowance and expenses, was approximately $3,726,000.
A final prospectus relating to this Offering was filed with the Commission on September 16, 2024. The shares of Common Stock were
approved to list on the NYSE American under the symbol “IBO” and began trading there on September 16, 2024. The Company
also issued warrants to the Representative and its affiliates (the “Representative’s Warrants”) warrants to
purchase the number of shares of Common Stock in the aggregate equal to 5%
of the Common Stock to be issued and sold in this offering (including any Shares of Common Stock sold upon exercise of the
over-allotment option, if applicable). The Representative’s Warrants are exercisable for a price per share equal to 125%
of the public offering price. The warrants are exercisable at any time, in whole or in part, commencing nine (9) months from the
date of commencement of sales of the offering and ending on the third anniversary thereof. As of September 30, 2024, the
Representative had not exercised any of these warrants. As of September 30, 2024, only the 1,500,000
shares included in the Offering are freely tradable on the NYSE. The remaining 9,997,703
are restricted from trading for 180 days from the Offering date.
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- DefinitionThe entire disclosure for equity.
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v3.24.3
Related Party Transactions
|
9 Months Ended |
Sep. 30, 2024 |
Related Party Transactions [Abstract] |
|
Related Party Transactions |
Note
10. Related Party Transactions
Research
and Development Activities
Based
on a shareholders agreement entered into on April 26, 2017, the Company would fund the scientific operations of GRDG, a company involved
in research and development of biomedical products which is a minority stockholder of two of the Company’s subsidiaries and is
owned by Daryl Thompson, a former director of many subsidiaries of the Company, to do the development and research works on the biomedical
products for the Company. On February 15, 2022, the Company and its subsidiaries, Global BioLife, Inc. (“Global”), and Impact
BioLife Sciences, Inc. (“BioLife Sciences”), and GRDG entered into a Licensing Proceeds Distribution Agreement (“GRDG
Agreement”), whereas GRDG would transfer its 20% equity position in both Global and BioLife Sciences to the Company in exchange
for 20% interest in Global and/or BioLife Science revenue received from the exclusive or non-exclusive licensing of and/or the sale of
Global Intellectual Property to a Third Party, net of specific costs. As of the date of this report, no contingent liability has been
recognized under the GRDG Agreement. The research and development agreement as well as the licensing proceeds distribution agreement
with GRDG were terminated in 2023. As of September 30, 2023, the Company incurred approximately $258,000 in expenses, and had approximately
$25,000 in prepaid monthly fees. For the nine months ended September 30, 2024, the Company had incurred $25,000 in fees.
General
and Administrative Costs
There
are certain general and administrative costs incurred by DSS, a related party, on behalf of the Company which are passed through to the
Company on a monthly basis. These costs consist of primarily payroll costs for certain DSS employees and are allocated based on estimated
time spent on behalf of the Company. Beginning in January 2024, these costs are approximately $31,000 per month. As of September 30,
2024, the Company incurred approximately $265,000 in related expenses. As of September 30, 2023, the Company incurred approximately $108,000
in related expenses
Note
payable, related party
On December 31, 2020, and later amended, the Company
executed a Revolving Promissory Note (“Note”) with DSS, a related party, which accrues interest at a rate of 4.25% and is
due in full at the maturity date of September 30, 2030. The Note was further amended on July 24, 2024 with an effective date of September
16, 2024 to i) allow the Company to pay certain principal and/or interest payments owing under the repayment terms in an exchange of equity
in the Company, ii) change the quarterly interest due dates to the last day of each calendar quarter (i.e. December 31, March 31, June
30 and September 30), iii) to partially eliminate the “On Demand, if No Demand” feature so that the “On Demand, if
no Demand” feature only starts after the 24th month, iv) continue the planned repayment program commencing on the 37th month and
on the last day of each month thereafter through August 31, 2030 to pay a fixed monthly payment of $126,381,
v) to continue the scheduled maturity date of September 30, 2030, and vi) adjusts the interest rate to be the WSJ Prime Rate plus 0.50%.
As of September 30, 2024 and December 31, 2023 the outstanding balance, inclusive of interest was $8,006,000 (net of change in fair value
of embedded derivative of $5,670,000) and $12,074,000, respectively. Of the $8,006,000, $35,000 is included in Current portion of note
payable, related party and the remaining $7,971,000 is included in Long-term portion of note payable, related party at September
30, 2024. The $12,074,000 at December 31, 2024 is included
in Current portion of note payable, related party (see Note 7).
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
|
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v3.24.3
Commitments and Contingencies
|
9 Months Ended |
Sep. 30, 2024 |
Commitments and Contingencies Disclosure [Abstract] |
|
Commitments and Contingencies |
Note
11. Commitments and Contingencies
On
August 15, 2018, the Company entered into Royalty Agreement with Chemia Corporation (“Chemia”) pursuant to which Chemia transferred
to the Company all of its right to 3F (Functional Fragrance Formulation). This agreement has a 20-year term and auto renews for a period
of 1 year unless mutually agreed upon by both parties. 3F consists of 3F Mosquito Repellant and 3F Anti-Viral formulations. Based on
the Royalty Agreement, the Company should cover all the costs to prepare and finalize necessary patent application and other intellectual
property related to 3F. Chemia agreed to support the Company in efforts leading to development of 3F intellectual property and it is
licensing. Based on Royalty Agreement any payments received from development, sales, licensing or transfer of 3F technology will be paid
50% to the Company and 50% to Chemia. On November 27, 2018, Company and Chemia signed an Addendum to Royalty Agreement (“Addendum”),
according to which the Company granted Chemia a royalty-based limited license for purposes of making and selling fragrances embodying
the 3F technology. Based on the Addendum, Chemia should pay the Company 5% of net sales in royalty. On November 8, 2019, both companies
entered into Amendment no.1 to Royalty Agreement, based on which certain expenses borne by the Company towards patent application and
licensing should be reimbursed to the Company before any royalty payments are made. For the three and nine months ended September 30,
2024 and 2023, there were no reimbursements or royalties paid to the Company and the Company cannot be assured that Chemia’s efforts
will end up in any future sales of the technology.
On
February 15, 2022, the Company and its subsidiaries, Global BioLife, Inc. (“Global”), and Impact BioLife Sciences, Inc. (“BioLife
Sciences”), and GRDG entered into a Licensing Proceeds Distribution Agreement (“GRDG Agreement”), whereas GRDG would
transfer its 20% equity position in both Global and BioLife Sciences to the Company in exchange for 20% interest in Global and/or BioLife
Science revenue received from the exclusive or non-exclusive licensing of and/or the sale of Global Intellectual Property to a Third
Party, net of specific costs. This Licensing Agreement ended in September 2023 as core technologies achieved significant development
milestones.
On
March 19, 2022, Impact BioMedical entered into a License Agreement (“Equivir License”) with a third-party (“Licensee”)
where the Licensor is granted the right, amongst other things, to develop, commercialize, and sell the Company’s Equivir technology.
In exchange, the Licensee shall pay the Company a royalty of 5.5% of net sales. Under the terms of the Equivir Agreement, the Company
shall reimburse the Licensee for 50% of the development costs provided that the development costs shall not exceed $1,250,000. As of
September 30, 2024 and December 31, 2023, a liability of $0 and $200,000, respectively, has been recorded in relation to the Equivir
License.
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v3.24.3
Subsequent Events
|
9 Months Ended |
Sep. 30, 2024 |
Subsequent Events [Abstract] |
|
Subsequent Events |
Note
12. Subsequent Events
The
Company has evaluated all other subsequent events and transactions through November 12, 2024, the date that the consolidated financial
statements were available to be issued and noted no other subsequent events requiring financial statement recognition or disclosure.
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v3.24.3
Summary of Significant Accounting and Reporting Policies (Policies)
|
9 Months Ended |
Sep. 30, 2024 |
Accounting Policies [Abstract] |
|
Basis of Presentation and Principles of Consolidation |
Basis
of Presentation and Principles of Consolidation
The
Company’s consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the
United States of America (“U.S. GAAP”). The consolidated financial statements include all accounts of the Company and its
majority owned and controlled subsidiaries. The Company consolidates entities in which it owns more than 50% of the voting common stock
and controls operations. All intercompany transactions and balances among consolidated subsidiaries have been eliminated. Non–controlling
interest represents the minority equity investment in the Company’s subsidiaries, plus the minority investors’ share of the
net operating results and other components of equity relating to the non–controlling interest.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
The
consolidated financial statements include all accounts of the entities as of the reporting period ending dates and for the reporting
periods as follows:
Schedule
of Condensed Financial Statements
Name of consolidated
subsidiary | |
State or other
jurisdiction of
incorporation or
organization | |
Date of incorporation
or formation | |
Attributable
interest as of
September 30, 2024 | | |
Attributable
interest as of
December 31, 2023 | |
| |
| |
| |
| | |
| |
Global BioMedical, Inc. | |
Nevada | |
April 18, 2017 | |
| 90.9 | % | |
| 90.9 | % |
Global BioLife, Inc. | |
Nevada | |
April 14, 2017 | |
| 81.8 | % | |
| 81.8 | % |
BioLife Sugar, Inc | |
Nevada | |
April 23, 2018 | |
| 90.9 | % | |
| 90.9 | % |
Happy Sugar Inc | |
Nevada | |
August 17, 2018 | |
| 81.8 | % | |
| 81.8 | % |
Sweet Sense Inc. | |
Nevada | |
April 30, 2018 | |
| 95.5 | % | |
| 95.5 | % |
Global Sugar Solutions Inc. | |
Nevada | |
November 7, 2019 | |
| 100 | % | |
| 100 | % |
As
of September 30, 2024, and December 31, 2023, the aggregate noncontrolling interest was equity of $3,003,000 and $3,040,000,
respectively, which are separately disclosed on the Consolidated Balance Sheets.
|
Use of estimates |
Use
of estimates
The
preparation of consolidated financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that
affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities as of the dates of the balance
sheets and reported amounts of revenues and expenses during the reporting periods. Actual results could differ from these estimates.
|
Reclassifications |
Reclassifications
Costs
associate with Sales and marketing have been reclassed from Other operating expenses for the three and nine months ended September 30,
2023 to conform with current period presentation. Also, cost associated with Professional fees for the three and nine months ended September 30, 2023 and the nine
months September 30, 2024 have been reclassified to Research and development to conform with current period presentation.
|
Loss per Share |
Loss
per Share
Basic
loss per share is computed by dividing the net loss attributable to the common stockholders by weighted average number of shares of common
stock outstanding during the period. Fully diluted loss per share is computed like basic loss per share except that the denominator is
increased to include the number of additional common shares that would have been outstanding if the potential common shares had been
issued and if the additional common shares were dilutive. There were no dilutive financial instruments issued or outstanding for the
three and nine months ended September 30, 2023. For the three and nine months ending September 30, 2024, there are 60,496,041 shares of Series A Convertible Preferred
Shares which are not eligible for conversion until April 10, 2027.
|
Fair Value of Financial Instruments |
Fair
Value of Financial Instruments
Fair
value is defined as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between
market participants at the measurement date. The Fair Value Measurement Topic of the Financial Accounting Standards Board (“FASB”)
Accounting Standards Codification (“ASC”) establishes a three-tier fair value hierarchy which prioritizes the inputs used
in measuring fair value. The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical assets
or liabilities (Level 1 measurements) and the lowest priority to unobservable inputs (Level 3 measurements). These tiers include:
●
Level 1, defined as observable inputs such as quoted prices for identical instruments in active markets,
●
Level 2, defined as inputs other than quoted prices in active markets that are either directly or indirectly observable such as quoted
prices for similar instruments in active markets or quoted prices for identical or similar instruments in markets that are not active;
and
●
Level 3, defined as unobservable inputs in which little or no market data exists, therefore requiring an entity to develop its own assumptions,
such as valuations derived from valuation techniques in which one or more significant inputs or significant value drivers are unobservable.
The
carrying amounts reported in the balance sheet of cash and cash equivalents, prepaids, accounts payable and accrued expenses approximate
fair value because of the immediate or short-term maturity of these financial instruments. The fair value of notes receivable approximates
their carrying value as the stated or discounted rates of the notes do reflect recent market conditions. The Company’s investments
are recorded at cost as the fair value of these investment in is not readily available. The fair value of notes payable approximates
its carrying value as the stated interest rate reflects recent market conditions.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
|
Cash and cash equivalents |
Cash
and cash equivalents
The
Company considers all highly liquid investments with a maturity of three months or less at the date of acquisition to be cash equivalents.
There were no cash equivalents as of September 30, 2024 and December 31, 2023.
|
Notes receivable, unearned interest, and related recognition |
Notes
receivable, unearned interest, and related recognition
The
Company records all future payments of principal and interest on notes as notes receivable, which are then offset by the amount of any
related unearned interest income. For financial statement purposes, the Company reports the net investment in the notes receivable on
the consolidated balance sheet as current or long-term based on the maturity date of the underlying notes. Such net investment is comprised
of the amount advanced on the loans, adjusting for net deferred loan fees or costs incurred at origination, amounts allocated to warrants
received upon origination, and any payments received in advance, if applicable. The unearned interest is recognized over the term of
the notes and the income portion of each note payment is calculated so as to generate a constant rate of return on the net balance outstanding.
If applicable, any net deferred loan fees or costs, together with discounts recognized in connection with warrants acquired at origination,
are accreted as an adjustment to yield over the term of the loan. (Note 3)
|
Goodwill |
Goodwill
Goodwill
is the excess of cost of an acquired entity over the fair value of amounts assigned to assets acquired and liabilities assumed in a business
combination. Goodwill is subject to impairment testing at least annually and will be tested for impairment between annual tests, which
will take place during the fourth quarter in 2024, if an event occurs or circumstances change that would indicate the carrying amount
may be impaired. FASB ASC Topic 350 provides an entity with the option to first assess qualitative factors to determine whether the existence
of events or circumstances leads to a determination that it is more likely than not that the fair value of a reporting unit is less than
its carrying amount. Some of the qualitative factors considered in applying this test include consideration of macroeconomic conditions,
industry and market conditions, cost factors affecting the business, and overall financial performance of the business. If, after completing
the assessment, it is determined that it is more likely than not that the fair value of a reporting unit is less than its carrying value,
the Company will proceed to a quantitative test. If qualitative factors are not deemed sufficient to conclude that the fair value of
the reporting unit more likely than not exceeds its carrying value, then a one-step approach is applied in making an evaluation. The
evaluation utilizes an income approach (discounted cash flow analysis). The computations require management to make significant estimates
and assumptions, including, among other things, selection of comparable publicly traded companies, the discount rate applied to future
earnings reflecting a weighted average cost of capital, and earnings growth assumptions. The Company believes the estimates and assumptions
used in our impairment assessments are reasonable and based on available market information, but variations in any of the assumptions
could result in materially different calculations of fair value and determinations of whether or not an impairment is indicated. A discounted
cash flow analysis requires management to make various assumptions about future sales, operating margins, capital expenditures, working
capital, and growth rates. Cash flow projections are derived from one-year budgeted amounts plus an estimate of later period cash flows,
all of which are determined by management. Subsequent period cash flows are developed for each reporting unit using growth rates that
management believes are reasonably likely to occur. Impairment of goodwill is measured as the excess of the carrying amount of goodwill
over the fair values of recognized and unrecognized assets and liabilities of the reporting unit. No impairment was recognized during
the three or nine months ended September 30, 2024 and 2023. (Note 5)
|
Intangible Assets |
Intangible
Assets
The
estimated fair values of acquired intangibles are generally determined based upon future economic benefits such as earnings and cash
flows. Acquired identifiable intangible assets are recorded at fair value and are amortized over their estimated useful lives. Acquired
intangible assets with an indefinite life are not amortized but are reviewed for impairment at least annually as of December 31st,
or more frequently whenever events or changes in circumstances indicate that the carrying amounts of those assets are below their estimated
fair values. Impairment is tested under ASC 350. No impairment was recognized for the three or nine months ended September 30, 2024,
and 2023. (Note 6)
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
|
Recoverability of Long-Lived Assets |
Recoverability
of Long-Lived Assets
We
evaluate long-lived assets such as property, equipment and definite lived intangible assets, such as patents, for impairment whenever
events or circumstances indicate that the carrying value of the assets recognized in our financial statements may not be recoverable.
Factors that we consider include whether there has been a significant decrease in the market value of an asset, a significant change
in the way an asset is being utilized, or a significant change, delay or departure in our strategy for that asset, or a significant change
in the macroeconomic environment. Our assessment of the recoverability of long-lived assets involves significant judgment and estimation.
These assessments reflect our assumptions, which, we believe, are consistent with the assumptions hypothetical marketplace participants
use. Factors that we must estimate when performing recoverability and impairment tests include, among others, forecasted revenue, margin
costs and the economic life of the asset. If impairment is indicated, we determine if the total estimated future cash flows on an undiscounted
basis are less than the carrying amounts of the asset or assets. If so, an impairment loss is measured and recognized.
Our
impairment loss calculations require that we apply judgment in identifying asset groups, estimating future cash flows, determining asset
fair values, and estimating asset’s useful lives. The Company reviews identifiable amortizable intangible assets for impairment
whenever events or changes in circumstances indicate that the carrying value of the assets may not be recoverable. Determination of recoverability
is based on the lowest level of identifiable estimated undiscounted cash flows resulting from use of the asset and its eventual disposition.
Measurement of any impairment loss is based on the excess of the carrying value of the asset over its fair value. Based on the uncertainty
of forecasts inherent with a new product, events such as the failure to generate forecasted revenue from new products could result in
a non-cash impairment in future periods.
|
Derivative Accounting |
Derivative Accounting
The Company analyzes all financial instruments with
features of both liabilities and equity under ASC 480, “Distinguishing Liabilities from Equity” and ASC 815, “Derivatives
and Hedging”. Derivative liabilities are adjusted to reflect fair value at each period end, with any increase or decrease
in the fair value being recorded in results of operations as adjustments to fair value of derivatives. The effects of interactions between
embedded derivatives are calculated and accounted for in arriving at the overall fair value of the financial instruments. Also, the fair
value of freestanding derivative instruments such as warrant and option derivatives are valued using the Black-Scholes simulation
model. The Company has determined that Note payable, related party contains an embedded derivative in the form of payment via equity and
has accounted for it in accordance with ASC 815. (see Note 7).
|
Revenue Recognition |
Revenue
Recognition
The
Company has adopted ASC Topic 606, Revenue from Contracts with Customers (“Topic 606”). The Company enters
into licensing and development agreements with collaborators for the development of its technologies. The terms of these agreements contain
multiple performance obligations which may include (i) licenses, or options to obtain licenses, to the Company’s technology, (ii)
rights to future technological improvements, and/or (iii) research activities to be performed on behalf of the collaborative partner.
Payments to the Company under these agreements may include upfront fees, option fees, exercise fees, payments based upon the achievement
of certain milestones, and royalties on product sales. Revenue is recognized when a customer obtains control of promised goods or services,
in an amount that reflects the consideration which the entity expects to receive in exchange for those goods or services. In determining
the appropriate amount of revenue to be recognized as it fulfills its obligations under the agreements, the Company performs the following
steps: (i) identification of the promised goods or services in the contract; (ii) determination of whether the promised goods or services
are performance obligations including whether they are distinct in the context of the contract; (iii) measurement of the transaction
price, including the constraint on variable consideration; (iv) allocation of the transaction price to the performance obligations; and
(v) recognition of revenue when or as the Company satisfies each performance obligation.
The
Company only applies the five-step model to contracts when it is probable that the Company will collect the consideration to which it
is entitled in exchange for the goods or services it transfers to the customer. At contract inception, once the contract is determined
to be within the scope of ASC 606, the Company assesses the goods or services promised within each contract and determines those that
are performance obligations and assesses whether each promised good or service is distinct. The Company then recognizes as revenue the
amount of the transaction price that is allocated to the respective performance obligation when or as the performance obligation is satisfied.
|
Research and Development |
Research
and Development
Research
and development costs are expensed as incurred. Total research and development costs were $386,000 for the nine months ended September
30, 2024, and $1,055,000 for nine months ended September 30, 2023.
IMPACT
Biomedical, Inc. and Subsidiaries
Notes
to Consolidated Financial Statements
|
Provision for Credit Losses |
Provision
for Credit Losses
On
January 1, 2022, the Company adopted amended accounting guidance “ASU No.2016-13 – Credit Losses” which requires
an allowance for credit losses to be deducted from the amortized cost basis of financial assets to present the net carrying value at
the amount that is expected to be collected over the contractual term of the asset considering relevant information about past events,
current conditions, and reasonable and supportable forecasts that affect the collectability of the reported amount. In estimating expected
losses in the loan and lease portfolio, borrower-specific financial data and macro-economic assumptions are utilized to project losses
over a reasonable and supportable forecast period. Assumptions and judgment are applied to measure amounts and timing of expected future
cash flows, collateral values and other factors used to determine the borrowers’ abilities to repay obligations. After the forecast
period, the Company utilizes longer-term historical loss experience to estimate losses over the remaining contractual life of the loans.
Prior to 2022, the allowance for credit losses represented the amount that in management’s judgment reflected incurred credit losses
inherent in the loan and lease portfolio as of the balance sheet date. As of September 30, 2024 and December 31, 2023 the Company has
deemed that no reserve on credit losses were necessary.
|
Continuing Operations and Going Concern |
Continuing
Operations and Going Concern
The
accompanying consolidated financial statements have been prepared assuming that the Company will continue as a going concern. This basis
of accounting contemplates the recovery of our assets and the satisfaction of liabilities in the normal course of business. As reflected
in the accompanying financial statements the Company has incurred operating losses as well as negative cash flows from operating and
investing activities over the past two years. These factors raise substantial doubt about the Company’s ability to continue as
a going concern within one year of the date that the financial statements are issued. These consolidated financial statements do not
include any adjustments to the specific amounts and classifications of assets and liabilities, which might be necessary should we be
unable to continue as a going concern.
To
continue as a going concern, the Company completed an initial public offering on September 16, 2024 raising $3,726,000
net of issuance costs and is currently listed on the NYSE American under the ticker symbol IBIO. The Company’s management
intends to take additional actions necessary to continue as a going concern. Management’s plans concerning these matters include,
among other things, monetization of its intellectual properties, and tightly controlling operating costs.
|
Recent Accounting Standards |
Recent
Accounting Standards
The
Financial Accounting Standards Board (FASB) issues various Accounting Standards Updates relating to the treatment and recording of certain
accounting transactions. There are several new accounting pronouncements issued by FASB which are not yet effective. Each of these pronouncements,
as applicable, has been or will be adopted by the Company. As of September 30, 2024, none of these pronouncements are expected to have
a material effect on the financial position, results of operations or cash flows of the Company.
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v3.24.3
Summary of Significant Accounting and Reporting Policies (Tables)
|
9 Months Ended |
Sep. 30, 2024 |
Accounting Policies [Abstract] |
|
Schedule of Condensed Financial Statements |
The
consolidated financial statements include all accounts of the entities as of the reporting period ending dates and for the reporting
periods as follows:
Schedule
of Condensed Financial Statements
Name of consolidated
subsidiary | |
State or other
jurisdiction of
incorporation or
organization | |
Date of incorporation
or formation | |
Attributable
interest as of
September 30, 2024 | | |
Attributable
interest as of
December 31, 2023 | |
| |
| |
| |
| | |
| |
Global BioMedical, Inc. | |
Nevada | |
April 18, 2017 | |
| 90.9 | % | |
| 90.9 | % |
Global BioLife, Inc. | |
Nevada | |
April 14, 2017 | |
| 81.8 | % | |
| 81.8 | % |
BioLife Sugar, Inc | |
Nevada | |
April 23, 2018 | |
| 90.9 | % | |
| 90.9 | % |
Happy Sugar Inc | |
Nevada | |
August 17, 2018 | |
| 81.8 | % | |
| 81.8 | % |
Sweet Sense Inc. | |
Nevada | |
April 30, 2018 | |
| 95.5 | % | |
| 95.5 | % |
Global Sugar Solutions Inc. | |
Nevada | |
November 7, 2019 | |
| 100 | % | |
| 100 | % |
|
X |
- DefinitionTabular disclosure of condensed financial statements, including, but not limited to, the balance sheet, income statement, and statement of cash flows.
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v3.24.3
Property, Plant and Equipment, Net (Tables)
|
9 Months Ended |
Sep. 30, 2024 |
Property, Plant and Equipment [Abstract] |
|
Schedule of Property Plant and Equipment |
Property,
plant and equipment consisted of the following as of:
Schedule
of Property Plant and Equipment
| |
Estimated | |
September 30, | | |
December 31, | |
| |
Useful Life | |
2024 | | |
2023 | |
Machinery and equipment | |
5-10 years | |
$ | 30,000 | | |
$ | 30,000 | |
Construction in progress | |
| |
| 263,000 | | |
| 263,000 | |
Total Cost | |
| |
| 293,000 | | |
| 293,000 | |
Less accumulated depreciation | |
| |
| 11,000 | | |
| 6,000 | |
Property, plant and equipment, net | |
| |
$ | 282,000 | | |
$ | 287,000 | |
|
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v3.24.3
Goodwill (Tables)
|
9 Months Ended |
Sep. 30, 2024 |
Goodwill and Intangible Assets Disclosure [Abstract] |
|
Schedule of Goodwill |
Goodwill
balances and activity for the nine months ended September 30, 2024 and year ended December 31, 2023 consisted of the following:
Schedule
of Goodwill
| |
| | |
Balance at December 31, 2023 | |
$ | 25,093,000 | |
Goodwill adjustment | |
| - | |
Balance at September 30, 2024 | |
$ | 25,093,000 | |
|
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v3.24.3
Intangible Assets (Tables)
|
9 Months Ended |
Sep. 30, 2024 |
Goodwill and Intangible Assets Disclosure [Abstract] |
|
Schedule of Intangible Assets |
The
definite-lived intangible assets, to be amortized over 20 years, balances, and activity for the nine months ended September 30, 2024
and year ended December 31, 2023 consisted of the following:
Schedule
of Intangible Assets
| |
September 30, 2024 | | |
December 31, 2023 | |
| |
Gross
Carrying Amount | | |
Accumulated Amortization | | |
Net
Carrying Amount | | |
Gross
Carrying Amount | | |
Accumulated Amortization | | |
Net
Carrying Amount | |
Definitive-lived: | |
| | | |
| | | |
| | | |
| | | |
| | | |
| | |
Developed technology | |
$ | 22,260,000 | | |
$ | (4,174,000 | ) | |
$ | 18,086,000 | | |
$ | 22,260,000 | | |
$ | (3,339,000 | ) | |
$ | 18,921,000 | |
Total | |
$ | 22,260,000 | | |
$ | (4,174,000 | ) | |
$ | 18,086,000 | | |
$ | 22,260,000 | | |
$ | (3,339,000 | ) | |
$ | 18,921,000 | |
|
Schedule of Future Amortization of Developed Technologies |
The
following table represents future amortization of developed technologies for the years ending December 31:
Schedule
of Future Amortization of Developed Technologies
| |
| | |
2024 | |
$ | 279,000 | |
2025 | |
$ | 1,113,000 | |
2026 | |
$ | 1,113,000 | |
2027 | |
$ | 1,113,000 | |
2028 | |
$ | 1,113,000 | |
Thereafter | |
$ | 13,355,000 | |
|
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v3.24.3
Note payable, related party (Tables)
|
9 Months Ended |
Sep. 30, 2024 |
Debt Disclosure [Abstract] |
|
Schedule of Principal Payments of Long-term Debt |
A
summary of scheduled principal payments of long-term debt (exclusive of the embedded derivative of $5,670,000), subsequent to September 30,
2024, are as follows:
Schedule
of Principal Payments of Long-term Debt
Year | | |
Amount | |
| 2024 | | |
$ | 35,000 | |
| 2025 | | |
| 781,000 | |
| 2026 | | |
| 12,860,000 | |
|
Schedule of Movement of Liability and Derivative Components of Note Payable |
The
movement in the liability and derivative components of the Note payable, related party as of December 31,2023 and September 30, 2024
are set out below:
Schedule of Movement of Liability and
Derivative Components of Note Payable
| |
Liability Component | | |
Derivative Component | | |
Total | |
December 31, 2023 | |
$ | 12,074,000 | | |
$ | - | | |
$ | 12,074,000 | |
Change in fair value of embedded derivative | |
| (7,098,000 | ) | |
| 1,428,000 | | |
| (5,670,000 | ) |
Advances on note | |
| 807,000 | | |
| - | | |
| 807,000 | |
Interest expense | |
| 795,000 | | |
| - | | |
| 795,000 | |
September 30, 2024 | |
$ | 6,578,000 | | |
$ | 1,428,000 | | |
$ | 8,006,000 | |
|
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v3.24.3
Financial Instruments (Tables)
|
9 Months Ended |
Sep. 30, 2024 |
Investments, All Other Investments [Abstract] |
|
Schedule of Cash, Cash Equivalents, Restricted Cash, and Note Payable Related Party by Significant Investment Category |
The following tables show the Company’s cash,
cash equivalents, restricted cash, and note payable, related party by significant investment category as of:
Schedule of Cash,
Cash Equivalents, Restricted Cash, and Note Payable Related Party by Significant Investment Category
| |
September 30, 2024 |
|
| |
Adjusted
cost | | |
Unrealized Gain/(Loss) | | |
Fair Value | | |
Cash and Cash Equivalents | |
|
Note
Payable,
Related Party |
|
Cash | |
$ | 2,668,000 | | |
$ | - | | |
$ | 2,668,000 | | |
$ | 2,668,000 | |
|
$ |
- |
|
Level 2 | |
| | | |
| | | |
| | | |
| | |
|
|
|
|
Note payble, related party | |
| 13,676,000 | | |
| (5,670,000 | ) | |
| 8,006,000 | | |
| - | |
|
|
8,006,000 |
|
Total | |
$ | 16,344,000 | | |
$ | (5,670,000 | ) | |
$ | 10,674,000 | | |
$ | 2,668,000 | |
|
$ |
8,006,000 |
|
| |
September 30, 2023 | |
| |
Adjusted Cost | | |
Unrealized Gain/(Loss) | | |
Fair Value | | |
Cash and Cash Equivalents | |
Cash | |
$ | 1,000 | | |
$ | - | | |
$ | 1,000 | | |
$ | 1,000 | |
Total | |
$ | 1,000 | | |
$ | - | | |
$ | 1,000 | | |
$ | 1,000 | |
|
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v3.24.3
Summary of Significant Accounting and Reporting Policies (Details Narrative) - USD ($)
|
|
3 Months Ended |
9 Months Ended |
|
Sep. 16, 2024 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Dec. 31, 2023 |
Noncontrolling interest |
|
$ 3,003,000
|
|
$ 3,003,000
|
|
$ 3,040,000
|
Cash equivalents |
|
0
|
|
0
|
|
0
|
Impairment of goodwill |
|
0
|
$ 0
|
0
|
$ 0
|
|
Impairment of intangible assets |
|
0
|
0
|
0
|
0
|
|
Research and development cost |
|
$ 82,000
|
$ 357,000
|
$ 386,000
|
$ 1,055,000
|
|
IPO [Member] |
|
|
|
|
|
|
Proceeds from Issuance Initial Public Offering |
$ 3,726,000
|
|
|
|
|
|
Series A Preferred Stock [Member] |
|
|
|
|
|
|
Convertible preferred shares |
|
60,496,041
|
|
60,496,041
|
|
|
Subsidiaries [Member] |
|
|
|
|
|
|
Noncontrolling interest |
|
$ 3,003,000
|
|
$ 3,003,000
|
|
$ 3,040,000
|
Sweet Sense Inc. [Member] |
|
|
|
|
|
|
Minority interest ownership percentage |
|
50.00%
|
|
50.00%
|
|
|
X |
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v3.24.3
Notes Receivable (Details Narrative) - USD ($)
|
Feb. 19, 2021 |
Sep. 30, 2024 |
Dec. 31, 2023 |
Dec. 31, 2020 |
Receivables [Abstract] |
|
|
|
|
Notes receivable current |
$ 206,000
|
$ 201,000
|
$ 203,000
|
|
Interest rate percentage |
6.50%
|
|
|
0.50%
|
Debt maturity date |
August 19, 2022 later amended to February 19, 2026
|
|
|
|
Current portion of notes receivable |
|
142,000
|
203,000
|
|
Note receivable |
|
$ 59,000
|
|
|
X |
- DefinitionContractual interest rate for funds borrowed, under the debt agreement.
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v3.24.3
Schedule of Property Plant and Equipment (Details) - USD ($)
|
Sep. 30, 2024 |
Dec. 31, 2023 |
Property, Plant and Equipment [Line Items] |
|
|
Total Cost |
$ 293,000
|
$ 293,000
|
Less accumulated depreciation |
11,000
|
6,000
|
Property, plant and equipment, net |
282,000
|
287,000
|
Machinery and Equipment [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Total Cost |
$ 30,000
|
30,000
|
Machinery and Equipment [Member] | Minimum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Estimated useful life |
5 years
|
|
Machinery and Equipment [Member] | Maximum [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Estimated useful life |
10 years
|
|
Construction in Progress [Member] |
|
|
Property, Plant and Equipment [Line Items] |
|
|
Total Cost |
$ 263,000
|
$ 263,000
|
X |
- DefinitionAmount of accumulated depreciation, depletion and amortization for physical assets used in the normal conduct of business to produce goods and services.
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Goodwill (Details Narrative) - USD ($)
|
Sep. 30, 2024 |
Dec. 31, 2023 |
Sep. 30, 2023 |
Credit Derivatives [Line Items] |
|
|
|
Initial value |
$ 25,093,000
|
$ 25,093,000
|
$ 46,400,000
|
Cash |
|
|
201,000
|
Business enterprise value |
|
|
46,600,000
|
Interest-bearing debt |
|
|
11,900,000
|
Fair value, common equity |
|
|
34,700,000
|
Fair value |
|
|
$ 5,100,000
|
Equity value exceeded carrying amount, percentage |
|
|
14.70%
|
Valuation, Market Approach [Member] |
|
|
|
Credit Derivatives [Line Items] |
|
|
|
Initial value |
|
|
$ 49,800,000
|
Weighted market approach percentage |
|
|
30.00%
|
Valuation, Income Approach [Member] |
|
|
|
Credit Derivatives [Line Items] |
|
|
|
Initial value |
|
|
$ 44,900,000
|
Weighted income approach percentage |
|
|
70.00%
|
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v3.24.3
Schedule of Intangible Assets (Details) - USD ($)
|
Sep. 30, 2024 |
Dec. 31, 2023 |
Finite-Lived Intangible Assets [Line Items] |
|
|
Gross carrying amount |
$ 22,260,000
|
$ 22,260,000
|
Accumulated amortization |
(4,174,000)
|
(3,339,000)
|
Net carrying amount |
18,086,000
|
18,921,000
|
Developed Technology Rights [Member] |
|
|
Finite-Lived Intangible Assets [Line Items] |
|
|
Gross carrying amount |
22,260,000
|
22,260,000
|
Accumulated amortization |
(4,174,000)
|
(3,339,000)
|
Net carrying amount |
$ 18,086,000
|
$ 18,921,000
|
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v3.24.3
Schedule of Future Amortization of Developed Technologies (Details)
|
Sep. 30, 2024
USD ($)
|
Goodwill and Intangible Assets Disclosure [Abstract] |
|
2024 |
$ 279,000
|
2025 |
1,113,000
|
2026 |
1,113,000
|
2027 |
1,113,000
|
2028 |
1,113,000
|
Thereafter |
$ 13,355,000
|
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v3.24.3
Schedule of Principal Payments of Long-term Debt (Details) - USD ($)
|
3 Months Ended |
9 Months Ended |
Sep. 30, 2024 |
Sep. 30, 2023 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Debt Disclosure [Abstract] |
|
|
|
|
Embedded Derivative, Gain (Loss) on Embedded Derivative, Net |
$ 5,670,000
|
|
$ 5,670,000
|
|
2024 |
35,000
|
|
35,000
|
|
2025 |
781,000
|
|
781,000
|
|
2026 |
$ 12,860,000
|
|
$ 12,860,000
|
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v3.24.3
Schedule of Movement of Liability and Derivative Components of Note Payable (Details) - USD ($)
|
3 Months Ended |
9 Months Ended |
Sep. 30, 2024 |
Sep. 30, 2023 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Short-Term Debt [Line Items] |
|
|
|
|
December 31, 2023 |
|
|
$ 12,074,000
|
|
Change in fair value of embedded derivative |
$ 5,670,000
|
|
5,670,000
|
|
Related Party [Member] |
|
|
|
|
Short-Term Debt [Line Items] |
|
|
|
|
December 31, 2023 |
|
|
12,074,000
|
|
Change in fair value of embedded derivative |
|
|
(5,670,000)
|
|
Advances on note |
|
|
807,000
|
|
Interest expense |
|
|
795,000
|
|
September 30, 2024 |
8,006,000
|
|
8,006,000
|
|
Liability Component [Member] |
|
|
|
|
Short-Term Debt [Line Items] |
|
|
|
|
September 30, 2024 |
8,006,000
|
|
8,006,000
|
|
Liability Component [Member] | Related Party [Member] |
|
|
|
|
Short-Term Debt [Line Items] |
|
|
|
|
December 31, 2023 |
|
|
12,074,000
|
|
Change in fair value of embedded derivative |
|
|
(7,098,000)
|
|
Advances on note |
|
|
807,000
|
|
Interest expense |
|
|
795,000
|
|
September 30, 2024 |
6,578,000
|
|
6,578,000
|
|
Derivative Component [Member] | Related Party [Member] |
|
|
|
|
Short-Term Debt [Line Items] |
|
|
|
|
December 31, 2023 |
|
|
|
|
Change in fair value of embedded derivative |
|
|
1,428,000
|
|
Advances on note |
|
|
|
|
Interest expense |
|
|
|
|
September 30, 2024 |
$ 1,428,000
|
|
$ 1,428,000
|
|
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- DefinitionNet Increase or Decrease in the fair value of the embedded derivative or group of embedded derivatives included in earnings in the period.
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v3.24.3
Note payable, related party (Details Narrative) - USD ($)
|
|
3 Months Ended |
9 Months Ended |
|
|
|
Dec. 31, 2020 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Dec. 31, 2024 |
Dec. 31, 2023 |
Feb. 19, 2021 |
Short-Term Debt [Line Items] |
|
|
|
|
|
|
|
|
Interest rate |
0.50%
|
|
|
|
|
|
|
6.50%
|
Fixed monthly payment |
$ 126,381
|
|
|
|
|
|
|
|
Notes payable |
|
|
|
|
|
$ 12,074,000
|
$ 12,074,000
|
|
Embedded Derivative, Gain (Loss) on Embedded Derivative, Net |
|
$ 5,670,000
|
|
$ 5,670,000
|
|
|
|
|
Note payable current |
|
35,000
|
|
35,000
|
|
|
12,074,000
|
|
Long term note payable |
|
$ 7,971,000
|
|
$ 7,971,000
|
|
|
|
|
Stock price |
|
$ 2.00
|
|
$ 2.00
|
|
|
$ 2.38
|
|
Related Party [Member] |
|
|
|
|
|
|
|
|
Short-Term Debt [Line Items] |
|
|
|
|
|
|
|
|
Notes payable |
|
$ 8,006,000
|
|
$ 8,006,000
|
|
|
$ 12,074,000
|
|
Embedded Derivative, Gain (Loss) on Embedded Derivative, Net |
|
|
|
(5,670,000)
|
|
|
|
|
Note payable current |
|
8,006,000
|
|
8,006,000
|
|
|
35,000
|
|
Long term note payable |
|
7,971,000
|
|
7,971,000
|
|
|
|
|
Revolving Promissory Note [Member] |
|
|
|
|
|
|
|
|
Short-Term Debt [Line Items] |
|
|
|
|
|
|
|
|
Interest rate |
4.25%
|
|
|
|
|
|
|
|
Debt instrument maturity date |
Sep. 30, 2030
|
|
|
|
|
|
|
|
Liability Component [Member] |
|
|
|
|
|
|
|
|
Short-Term Debt [Line Items] |
|
|
|
|
|
|
|
|
Notes payable |
|
8,006,000
|
|
8,006,000
|
|
|
|
|
Liability Component [Member] | Related Party [Member] |
|
|
|
|
|
|
|
|
Short-Term Debt [Line Items] |
|
|
|
|
|
|
|
|
Notes payable |
|
$ 6,578,000
|
|
6,578,000
|
|
|
$ 12,074,000
|
|
Embedded Derivative, Gain (Loss) on Embedded Derivative, Net |
|
|
|
$ (7,098,000)
|
|
|
|
|
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v3.24.3
Schedule of Cash, Cash Equivalents, Restricted Cash, and Note Payable Related Party by Significant Investment Category (Details) - USD ($)
|
Dec. 31, 2024 |
Sep. 30, 2024 |
Dec. 31, 2023 |
Sep. 30, 2023 |
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
|
|
Cash and cash Equivalents |
|
$ 2,668,000
|
$ 1,000
|
|
Cash and Cash Equivalents, Note payable, related party |
|
7,971,000
|
|
|
Note payable, related party |
$ 12,074,000
|
|
12,074,000
|
|
Related Party [Member] |
|
|
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
|
|
Cash and Cash Equivalents, Note payable, related party |
|
7,971,000
|
|
|
Note payable, related party |
|
8,006,000
|
$ 12,074,000
|
|
Fair Value, Recurring [Member] |
|
|
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
|
|
Cash and cash Equivalents |
|
2,668,000
|
|
$ 1,000
|
Unrealized Gain/(Loss) |
|
(5,670,000)
|
|
|
Note payable, related party |
|
8,006,000
|
|
|
Adjusted cost |
|
16,344,000
|
|
|
Fair Value |
|
10,674,000
|
|
|
Cash and Cash Equivalents |
|
2,668,000
|
|
|
Fair Value, Recurring [Member] | Fair Value, Inputs, Level 2 [Member] | Related Party [Member] |
|
|
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
|
|
Adjusted cost, Note payable, related party |
|
13,676,000
|
|
|
Unrealized Gain/(Loss) |
|
(5,670,000)
|
|
|
Fair Value, Note payable, related party |
|
8,006,000
|
|
|
Cash and Cash Equivalents, Note payable, related party |
|
|
|
|
Note payable, related party |
|
$ 8,006,000
|
|
|
X |
- DefinitionCash cash equivalents and marketable securities.
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v3.24.3
Stockholders’ Equity (Details Narrative) - USD ($)
|
|
|
|
|
|
9 Months Ended |
12 Months Ended |
|
|
|
Sep. 30, 2024 |
Sep. 17, 2024 |
Sep. 16, 2024 |
Oct. 31, 2023 |
May 10, 2023 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Oct. 31, 2024 |
Dec. 31, 2023 |
May 11, 2023 |
Dec. 31, 2022 |
Class of Stock [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
Common Stock, Shares Authorized |
4,000,000,000
|
|
|
|
|
4,000,000,000
|
|
|
4,000,000,000
|
|
|
Common stock, par value |
$ 0.001
|
|
|
|
|
$ 0.001
|
|
|
$ 0.001
|
|
|
Preferred Stock, Shares Authorized |
100,000,000
|
|
|
|
|
100,000,000
|
|
|
100,000,000
|
|
|
Preferred Stock, Par or Stated Value Per Share |
$ 0.001
|
|
|
|
|
$ 0.001
|
|
|
$ 0.001
|
|
|
Common stock shares outstanding |
11,503,955
|
|
|
|
125,073,621
|
11,503,955
|
|
|
10,000,000
|
3,877,282,251
|
|
Preferred Stock, Shares Outstanding |
60,496,041
|
|
|
|
0
|
60,496,041
|
|
|
60,496,041
|
0
|
|
Stockholders' equity, reverse stock split |
|
|
|
1 for 55
|
|
|
|
|
|
|
|
Preferred stock convertible shares issuable |
|
|
|
60,496,041
|
|
|
|
|
|
|
|
Common Stock, Conversion Basis |
|
|
|
Series
A Convertible Preferred Shares, reducing its ownership of the Company’s Common Stock from approximately 88% to approximately 12%.
|
|
|
|
Series A Convertible Preferred
Shares, reducing its ownership of the Company’s Common Stock from approximately 88% to approximately 12%
|
|
|
|
Common stock shares issued |
11,503,955
|
|
|
|
|
11,503,955
|
|
|
10,000,000
|
|
|
Preferred Stock, Shares Issued |
60,496,041
|
|
|
|
|
60,496,041
|
|
|
60,496,041
|
|
|
Shares converted |
|
|
|
|
|
70,496,041
|
|
|
|
|
|
Issuance of common stock, shares |
1,500,000
|
|
|
|
|
|
|
|
|
|
|
Issuance of common stock |
|
|
|
|
|
$ 3,726,000
|
|
|
|
|
|
Equity ownership percentage |
|
|
5.00%
|
|
|
|
|
|
|
|
|
Percentage of warrants exercisable |
|
|
125.00%
|
|
|
|
|
|
|
|
|
Restricted Stock or Unit Expense |
|
|
|
|
|
|
|
|
|
|
|
Class of Stock [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
Issuance of common stock, shares |
9,997,703
|
|
|
|
|
|
|
|
|
|
|
Underwriting Agreement [Member] |
|
|
|
|
|
|
|
|
|
|
|
Class of Stock [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
Common stock, par value |
|
|
$ 0.001
|
|
|
|
|
|
|
|
|
Issuance of common stock, shares |
|
|
1,500,000
|
|
|
|
|
|
|
|
|
Share price |
|
|
$ 3.00
|
|
|
|
|
|
|
|
|
Issuance of common stock |
|
$ 3,726,000
|
|
|
|
|
|
|
|
|
|
Common Stock [Member] |
|
|
|
|
|
|
|
|
|
|
|
Class of Stock [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
Common stock shares outstanding |
|
|
|
|
|
|
|
|
3,877,282,251
|
|
3,877,282,251
|
Common stock shares issued |
|
|
|
|
|
|
|
|
3,877,282,251
|
|
3,877,282,251
|
Series A Preferred Stock [Member] |
|
|
|
|
|
|
|
|
|
|
|
Class of Stock [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
Preferred stock convertible shares issuable |
|
|
|
60,496,041
|
|
|
|
|
|
|
|
Board of Directors Chairman [Member] |
|
|
|
|
|
|
|
|
|
|
|
Class of Stock [Line Items] |
|
|
|
|
|
|
|
|
|
|
|
Common Stock, Shares Authorized |
|
|
|
|
4,000,000,000
|
|
|
|
|
|
|
Common stock, par value |
|
|
|
|
$ 0.001
|
|
|
|
|
|
|
Common Stock, Voting Rights |
|
|
|
|
Each
share of Common Stock when issued, shall have one (1) vote on all matters presented to the stockholders.
|
|
|
|
|
|
|
Preferred Stock, Shares Authorized |
|
|
|
|
100,000,000
|
|
|
|
|
|
|
Preferred Stock, Par or Stated Value Per Share |
|
|
|
|
$ 0.001
|
|
|
|
|
|
|
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v3.24.3
Related Party Transactions (Details Narrative) - USD ($)
|
|
|
|
3 Months Ended |
9 Months Ended |
|
|
|
Jan. 01, 2024 |
Feb. 15, 2022 |
Dec. 31, 2020 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Sep. 30, 2024 |
Sep. 30, 2023 |
Dec. 31, 2024 |
Dec. 31, 2023 |
Feb. 19, 2021 |
Related Party Transaction [Line Items] |
|
|
|
|
|
|
|
|
|
|
Expenses |
|
|
|
$ 82,000
|
$ 357,000
|
$ 386,000
|
$ 1,055,000
|
|
|
|
Debt Instrument, Periodic Payment |
|
|
$ 126,381
|
|
|
|
|
|
|
|
Debt Instrument, Interest Rate, Stated Percentage |
|
|
0.50%
|
|
|
|
|
|
|
6.50%
|
Debt instrument description |
|
|
|
|
|
Of the $8,006,000, $35,000 is included in Current portion of note
payable, related party and the remaining $7,971,000 is included in Long-term portion of note payable, related party at September
30, 2024.
|
|
|
|
|
Notes Payable |
|
|
|
|
|
|
|
$ 12,074,000
|
$ 12,074,000
|
|
Revolving Promissory Note [Member] |
|
|
|
|
|
|
|
|
|
|
Related Party Transaction [Line Items] |
|
|
|
|
|
|
|
|
|
|
Debt Instrument, Interest Rate, Stated Percentage |
|
|
4.25%
|
|
|
|
|
|
|
|
Debt outstanding balance |
|
|
|
8,006,000
|
|
$ 8,006,000
|
|
|
$ 12,074,000
|
|
Change in fair value of embedded derivative |
|
|
|
5,670,000
|
|
5,670,000
|
|
|
|
|
GRDG Science LLC [Member] |
|
|
|
|
|
|
|
|
|
|
Related Party Transaction [Line Items] |
|
|
|
|
|
|
|
|
|
|
Expenses |
|
|
|
|
|
|
258,000
|
|
|
|
Prepaid monthly fees |
|
|
|
$ 25,000
|
$ 25,000
|
25,000
|
25,000
|
|
|
|
DSS Inc. [Member] |
|
|
|
|
|
|
|
|
|
|
Related Party Transaction [Line Items] |
|
|
|
|
|
|
|
|
|
|
Related costs for employees per month |
$ 31,000
|
|
|
|
|
|
|
|
|
|
General and administrative expense |
|
|
|
|
|
$ 265,000
|
$ 108,000
|
|
|
|
Global and BioLife Sciences [Member] |
|
|
|
|
|
|
|
|
|
|
Related Party Transaction [Line Items] |
|
|
|
|
|
|
|
|
|
|
Ownership percentage |
|
20.00%
|
|
|
|
|
|
|
|
|
Sale of royalty percentage |
|
20.00%
|
|
|
|
|
|
|
|
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v3.24.3
Commitments and Contingencies (Details Narrative) - USD ($)
|
Mar. 19, 2022 |
Feb. 15, 2022 |
Nov. 27, 2018 |
Aug. 15, 2018 |
Sep. 30, 2024 |
Dec. 31, 2023 |
Global and BioLife Sciences [Member] |
|
|
|
|
|
|
Sale of royalty percentage |
|
20.00%
|
|
|
|
|
Ownership percentage |
|
20.00%
|
|
|
|
|
Royalty Agreement [Member] |
|
|
|
|
|
|
Royalty percentage |
|
|
|
50.00%
|
|
|
Royalty Agreement [Member] | Chemia Corporation [Member] |
|
|
|
|
|
|
Royalty percentage |
|
|
|
50.00%
|
|
|
Sale of royalty percentage |
|
|
5.00%
|
|
|
|
License Agreement [Member] |
|
|
|
|
|
|
Sale of royalty percentage |
5.50%
|
|
|
|
|
|
Development cost, percent |
50.00%
|
|
|
|
|
|
Development costs |
$ 1,250,000
|
|
|
|
|
|
Accrued costs |
|
|
|
|
$ 0
|
$ 200,000
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