Announces Commercial Launch of Two New
Thrombectomy Devices for the Venous and Arterial Vasculatures:
Pounce™ Venous and Pounce LP (Low Profile)
Surmodics, Inc. (Nasdaq: SRDX), a leading provider of medical
device and in vitro diagnostic technologies to the healthcare
industry, today reported financial results for its second quarter
ended March 31, 2024, and updated financial guidance for its fiscal
year ending September 30, 2024.
Second Quarter Fiscal 2024 Financial Summary
- Total Revenue of $32.0 million, an increase of 18%
year-over-year
- Total Revenue excluding SurVeil™ drug-coated balloon (“DCB”)
license fee revenue(1) of $30.9 million, an increase of 19%
year-over-year
- GAAP net income of $0.2 million, compared to a net loss of
$(7.7) million in the prior-year period
- Adjusted EBITDA(2) of $4.8 million, compared to $(1.5) million
in the prior-year period
Second Quarter and Recent Business Highlights
- On January 22, 2024, Surmodics announced the successful early
clinical use and limited market evaluation (LME) of the Pounce LP
(Low Profile) Thrombectomy System, which is designed for removal of
acute-to-chronic thrombi and emboli in peripheral arteries ranging
from 2 mm to 4 mm, such as those found below the knee.
- Today, Surmodics is announcing the completion of LME and
commercial launch of two new mechanical thrombectomy systems for
the peripheral venous and arterial vasculatures, the Pounce Venous
Thrombectomy System and the Pounce LP Thrombectomy System.
- The Pounce Venous Thrombectomy System, which transitioned to
commercial launch in March, is designed to remove mixed-morphology,
wall-adherent peripheral venous clot in a single treatment session
while minimizing the need for thrombolytics.
- The Pounce LP Thrombectomy System, which transitioned to
commercial launch in April, addresses an important unmet need for
the prompt removal of acute-to-chronic thrombi or emboli in
below-the-knee arteries 2 to 4 mm in diameter while minimizing the
need for thrombolytics.
“I’m incredibly proud of our team’s impressive pace of execution
in the second quarter, which yielded strong financial performance
that exceeded our expectations, and progress with respect to all of
our stated strategic objectives for fiscal 2024,” said Gary
Maharaj, President and CEO of Surmodics, Inc. “Our total revenue
growth was fueled primarily by product sales growth of 40%
year-over-year in our Medical Device segment, where we were pleased
to see consistent demand for our SurVeil™ DCB – which was
commercialized by Abbott during the quarter – and strong sales of
our Pounce thrombectomy products. In combination with our continued
focus on controlling our expenses, our strong revenue performance
enabled us to achieve net income profitability in the second
quarter, and we ultimately generated over $7 million in cash flow
from operations to further strengthen our balance sheet, ending the
quarter with $41 million of cash and investments. Importantly, we
also made significant progress with respect to the limited market
evaluations for two new products, Pounce Venous Thrombectomy and
Pounce LP (Low Profile), and are excited to announce the full
commercial launch of both products today.”
Mr. Maharaj continued, “We are raising our revenue and EPS
guidance today for the second time this year, reflecting our
outperformance in the second quarter and improved outlook for the
balance of the fiscal year. With steady growth in our core
businesses, commercial traction in our existing vascular
interventions portfolio, and the recent introduction of four major
new products this year, we are well-positioned to deliver strong,
sustained revenue performance as we look ahead. In the second half
fiscal 2024, Surmodics remains focused on facilitating the adoption
of these important growth catalysts to capitalize on the
multi-billion-dollar market opportunity they collectively address,
while executing efficiently against our strategic initiatives and
allocating capital thoughtfully to enhance our underlying
profitability profile.”
Second Quarter Fiscal 2024 Financial Results
Three Months Ended March
31,
Increase (Decrease)
2024
2023
$
%
Revenue:
Medical Device
$
24,826
$
19,707
$
5,119
26
%
In Vitro Diagnostics
7,132
7,491
(359
)
(5
)%
Total revenue
$
31,958
$
27,198
$
4,760
18
%
Total revenue increased $4.8 million, or 18%, to $32.0 million,
compared to $27.2 million in the second quarter of fiscal 2023.
Excluding SurVeil DCB license fee revenue,(1) total revenue
increased $5.0 million, or 19%, to $30.9 million, compared to $25.9
million in the second quarter of fiscal 2023.
Medical Device revenue increased $5.1 million, or 26%, to $24.8
million, compared to $19.7 million in the second quarter of fiscal
2023. Excluding SurVeil DCB license fee revenue,(1) Medical Device
revenue increased $5.4 million, or 29% to $23.7 million, compared
to $18.4 million in the second quarter of fiscal 2023, primarily
driven by product sales and performance coating royalties and
license fee revenue. Medical Device product sales increased $3.2
million, or 40%, to $11.1 million, compared to $7.9 million in the
second quarter of fiscal 2023, driven primarily by commercial
shipments of the SurVeil DCB to Abbott Vascular, Inc. (“Abbott”),
the company’s exclusive distribution partner for the product, and
growth in sales of the Pounce thrombectomy device platform. Medical
Device performance coating royalties and license fee revenue
increased $2.2 million, or 27%, to $10.3 million, compared to $8.1
million in the second quarter of fiscal 2023, primarily driven by
$1.4 million in catch-up payments reported by customers and growth
in customer utilization of Surmodics’ hydrophilic coatings. IVD
revenue decreased $0.4 million, or 5%, to $7.1 million, compared to
$7.5 million in the second quarter of fiscal 2023, primarily driven
by lower sales of colorimetric substrate products.
Product gross profit(3) increased $1.4 million, or 14%, to $11.0
million, compared to $9.6 million in the second quarter of fiscal
2023. Product gross margin(3) was 60.8%, compared to 62.6% in the
second quarter of fiscal 2023. The decrease in product gross margin
was primarily driven by increased sales of SurVeil DCB, Pounce
thrombectomy and Sublime™ radial access products as a proportion of
total product sales, as these devices were not at scale, and
product gross margins reflected the associated under-absorption and
production inefficiencies.
Operating costs and expenses, excluding product costs, decreased
$3.8 million, or 14%, to $24.2 million, compared to $28.0 million
in the second quarter of fiscal 2023. The decrease was primarily
driven by lower research and development expenses due to the
transition of the SurVeil DCB to commercialization, the timing of
development and commercialization of the company’s thrombectomy
devices, and the spending reduction plan implemented in the second
quarter of fiscal 2023. In addition, the second quarter of fiscal
2023 included $1.3 million in severance-related restructuring
expense from the workforce restructuring implemented during the
period.
GAAP net income was $0.2 million, or $0.02 per diluted share,
compared to GAAP net loss of $(7.7) million, or $(0.55) per diluted
share in the second quarter of fiscal 2023. Non-GAAP net income(4)
was $1.1 million, or $0.07 per diluted share,(4) compared to
Non-GAAP net loss(4) of $(5.6) million, or $(0.40) per diluted
share(4) in the second quarter of fiscal 2023.
Adjusted EBITDA(2) was $4.8 million, compared to Adjusted
EBITDA(2) loss of $(1.5) million in the second quarter of fiscal
2023.
Balance Sheet Summary
As of March 31, 2024, Surmodics reported $40.9 million in cash
and investments, $5.0 million in outstanding borrowings on its
revolving credit facility, and $25.0 million in outstanding
borrowings on its term loan facility. The company had access to
approximately $65.0 million in additional debt capital as of March
31, 2024 under its revolving credit and term loan facilities.
Surmodics reported $7.4 million in cash provided by operating
activities and $1.3 million in capital expenditures in the second
quarter of fiscal 2024. In the second quarter of fiscal 2024, cash
and investments increased by $5.8 million, which consisted of the
change in the combined balance of cash and cash equivalents and
investments in available-for-sale securities from December 31, 2023
to March 31, 2024.
Fiscal Year 2024 Financial Guidance
Surmodics now expects fiscal 2024 total revenue to range from
$122 million to $124 million, representing a decrease of (8)% to
(6)% compared to fiscal 2023. Excluding SurVeil DCB license fee
revenue,(1) Surmodics expects fiscal 2024 total revenue to range
from $118 million to $120 million, representing an increase of 15%
to 17% compared to fiscal 2023. The company’s prior guidance called
for fiscal 2024 total revenue of $117 to $121 million, representing
a decrease of (12)% to (9)% compared to fiscal 2023, and total
revenue excluding SurVeil DCB license fee revenue(1) of $113
million to $117 million, representing an increase of 10% to 14%
compared to fiscal 2023.
The company now expects fiscal 2024 GAAP diluted loss per share
to range from $(0.90) to $(0.70). The company’s prior guidance
called for fiscal 2024 GAAP diluted loss per share to range from
$(1.40) to $(1.10).
Non-GAAP diluted loss per share(4) in fiscal 2024 is now
expected to range from $(0.67) to $(0.47). The company’s prior
guidance called for fiscal 2024 Non-GAAP diluted loss per share(4)
of $(1.17) to $(0.87).
Conference Call Today at 7:00 a.m. CT (8:00 a.m. ET)
Surmodics is hosting a live webcast at 7:00 a.m. CT (8:00 a.m.
ET) today to discuss second quarter of fiscal 2024 financial
results and accomplishments and host a question-and-answer session.
To access the webcast, please go to “Events & Presentations”
under the “Investors” section of the company’s website at
https://surmodics.gcs-web.com/events-and-presentations, and click
on the webcast icon under “Upcoming Events.” To listen to the live
teleconference, dial 800-407-8293 (international callers may dial
+1 201-689-8349) and provide event ID 13745933.
An audio replay of the conference call will be available
beginning at approximately 11:00 a.m. CT today, until approximately
11:00 a.m. CT on Wednesday, May 15, and can be accessed by dialing
877-660-6853 (international callers may dial +1 201-612-7415) and
entering access ID 13745933. In addition, the webcast and
transcript will be archived on the company’s website following the
call.
About the Pounce Venous Thrombectomy System
Surmodics’ Pounce Venous Thrombectomy System is a mechanical
thrombectomy system engineered specifically for the unique
requirements of the peripheral venous vasculature. The Pounce
Venous System, which Surmodics acquired from Vetex Medical Limited
in 2021, is indicated for mechanical de-clotting and controlled and
selective infusion of physician-specified fluids, including
thrombolytics, in the peripheral vasculature. The Pounce Venous
System (minimum 10 Fr) is designed to remove mixed-morphology,
wall-adherent venous clot in a single session, minimizing the need
for thrombolytics and without the need for capital equipment. It
may be used with the Pounce Sheath (12 Fr), which received FDA
510(k) clearance in September 2023 and is intended to introduce
therapeutic or diagnostic devices into the vasculature. The Pounce
Venous System’s dual-action technology consists of an adjustable
basket (3–4 cm in length) to collect clot and an inner extraction
screw to macerate and remove the clot. The wall-apposed basket
adapts to vessel size and may be collapsed at the physician’s
discretion to avoid contact with areas not targeted for
treatment.
In a prospective, European, first-in-human study(9) (n=19) of
the Pounce Venous Thrombectomy System in symptomatic iliofemoral
thrombus (≤14 days duration), 100% of procedures met the primary
performance endpoint of Society of Interventional Radiology (“SIR”)
Grade ≥II Lysis (50% to 95% thrombus removal) in the target vessel,
while no device-related adverse events or major bleeding were
reported. Only 2 of 11 patients available for 12-month follow-up
had mild post-thrombotic symptoms (Villalta Score 5–9), while none
had moderate or severe symptoms.
About the Pounce Thrombectomy Platform Indicated for Use in
Peripheral Arterial Vasculature
Surmodics’ Pounce Thrombectomy Platform, indicated for use in
peripheral vasculature, is a suite of mechanical thrombectomy
systems designed for the non-surgical removal of thrombi and
emboli. Two different-sized systems are available: the original
Pounce (mid profile) Thrombectomy System, indicated for use in
peripheral arterial vessels 3.5 mm to 6 mm in diameter, and the
Pounce LP (Low Profile) Thrombectomy System, indicated for use in
peripheral arterial vessels 2 mm to 4 mm in diameter. These systems
received FDA 510(k) clearance in July 2021 and June 2023,
respectively. The Pounce and Pounce LP Systems are fully mechanical
and designed to remove acute-to-chronic thrombi and emboli in
peripheral arteries without the need for capital equipment or
aspiration while minimizing the use of thrombolytics. As
“grab-and-go” solutions, the Pounce and Pounce LP Systems are
readily deployable and simple to use. Each system consists of three
components: a delivery catheter, the basket wire and a funnel
catheter. The basket wire is delivered distal to the location of
the thrombus, deploying two nitinol self-expanding baskets. The
baskets capture the clot and are retracted into the nitinol
collection funnel. With the clot entrained, the system is withdrawn
into a minimum 7 Fr guide sheath through which the clot is removed
from the body.
In a retrospective study(10) of 44 consecutive patients treated
using the original Pounce Thrombectomy System for lower extremity
limb ischemia with suspected thrombus (acute, subacute and chronic
clot), investigators achieved 83% success in effectively removing
thrombus from the arterial segments in which the device was used.
Adjunctive thrombolysis was used to resolve thrombus in just 2.3%
(1 of 44) of cases.
About Surmodics, Inc.
Surmodics, Inc. is a leading provider of performance coating
technologies for intravascular medical devices and chemical and
biological components for in vitro diagnostic immunoassay tests and
microarrays. Surmodics also develops and commercializes highly
differentiated vascular intervention medical devices that are
designed to address unmet clinical needs and engineered to the most
demanding requirements. This key growth strategy leverages the
combination of the company’s expertise in proprietary surface
modification and drug-delivery coating technologies, along with its
device design, development and manufacturing capabilities. The
company’s mission is to improve the detection and treatment of
disease. Surmodics is headquartered in Eden Prairie, Minnesota. For
more information, visit www.surmodics.com. The content of
Surmodics’ website is not part of this press release or part of any
filings that the company makes with the SEC.
Safe Harbor for Forward-looking Statements
This press release, and disclosures related to it, contain
forward-looking statements within the meaning of the Private
Securities Litigation Reform Act of 1995. Statements that are not
historical or current facts, including statements regarding: future
success; our focus on disciplined expense management and
optimization of working capital; our access to additional
borrowings under our existing credit agreement; our ability to
capitalize on the key near-term growth catalysts in our vascular
interventions portfolio by facilitating the adoption and
utilization of SurVeil DCB products, Pounce thrombectomy products,
and Sublime radial access products; the potential for Abbott’s
sales team to use the results of the TRANSCEND trial with potential
SurVeil DCB physician users; Abbott’s progress in the market as
they work to facilitate the adoption of the SurVeil DCB; our
ability to obtain long-term growth by developing and introducing
new products and line extensions to enhance our existing Pounce,
Sublime, and medical device performance coatings portfolios; the
likely key drivers of adoption of the Pounce Venous Thrombectomy
System; whether we will continue to enhance and strengthen our
position as an industry-leading provider of performance coating
technologies; our ability to obtain durable revenue growth and cash
flow generation across our core performance coatings and IVD
products; being well-capitalized to support future growth
objectives; expected full-year fiscal 2024 growth rates for our
performance coatings and IVD products; our fiscal 2024 financial
guidance and related statements and assumptions, including
statements regarding our ability to generate total revenue growth
for the full fiscal 2024 year, excluding SurVeil DCB license fees,
our ability to accelerate our total revenue growth profile in
fiscal 2024, assumptions in our revenue guidance provided for
modeling purposes, expected revenue associated with our Medical
Device performance coatings offerings and IVD business, expected
license fee revenue related to the SurVeil DCB, expected product
revenue as a percentage of total revenue, expected product revenue
from our SurVeil, Pounce, and Sublime products, expected product
gross margins for fiscal 2024, expected operating expenses,
expected interest expense, and expected tax expense; the range of
revenue we expect in the third quarter of fiscal 2024; our expected
total cash and investments balance at the end of fiscal 2024 and
expected sources and uses of cash in fiscal 2024; expectations
related to further borrowings during fiscal 2024 under our credit
agreement; our fiscal 2024 strategic objectives; being well
positions to achieve and deliver strong, sustained revenue growth;
and delivering sustained improvements in our underlying
profitability profile, are forward-looking statements.
Forward-looking statements involve inherent risks and
uncertainties, and important factors could cause actual results to
differ materially from those anticipated, including, without
limitation: (1) our ability to successfully commercialize our
SurVeil DCB (including realization of the full potential benefits
of our agreement with Abbott), Sundance DCB, and other proprietary
products; (2) our reliance on third parties (including our
customers and licensees) and their failure to successfully develop,
obtain regulatory approval for, market, and sell products
incorporating our technologies; (3) possible adverse market
conditions and possible adverse impacts on our cash flows; (4) our
ability to successfully and profitably produce and commercialize
our vascular intervention products; (5) supply chain constraints;
(6) whether our operating expenses are effective in generating
profitable revenues; (7) disruptions to our business from our plan
to reduce our use of cash announced in the second quarter of fiscal
2023, the failure of such plan to achieve its objectives, or cost
and expenses associated with such plan; and (8) the factors
identified under “Risk Factors” in Part I, Item 1A of our Annual
Report on Form 10-K for the fiscal year ended September 30, 2023
and subsequent SEC filings. These reports are available in the
Investors section of our website at https://surmodics.gcs-web.com
and at the SEC website at www.sec.gov. Forward-looking statements
speak only as of the date they are made, and we undertake no
obligation to update them in light of new information or future
events.
Use of Non-GAAP Financial Information
In addition to reporting financial results in accordance with
U.S. generally accepted accounting principles, or GAAP, Surmodics
is reporting non-GAAP financial results including total revenue
excluding SurVeil DCB license fee revenue, Medical Device revenue
excluding SurVeil DCB license fee revenue, EBITDA and Adjusted
EBITDA, non-GAAP operating income (loss), non-GAAP operating income
(loss) percentage, non-GAAP income (loss) before income taxes,
non-GAAP net income (loss), and non-GAAP income (loss) per diluted
share. We believe that these non-GAAP measures, when read in
conjunction with the company’s GAAP financial statements, provide
meaningful insight into our operating performance excluding certain
event-specific matters, and provide an alternative perspective of
our results of operations. We use non-GAAP measures, including
those set forth in this release, to assess our operating
performance and to determine payouts under our executive
compensation programs. We also are providing guidance on a range of
non-GAAP revenue and loss per diluted share for fiscal 2024. We
believe that presentation of certain non-GAAP measures allows
investors to review our results of operations from the same
perspective as management and our board of directors and
facilitates comparisons of our current results of operations. The
method we use to produce non-GAAP results is not in accordance with
GAAP and may differ from the methods used by other companies.
Non-GAAP results should not be regarded as a substitute for
corresponding GAAP measures but instead should be utilized as a
supplemental measure of operating performance in evaluating our
business. Non-GAAP measures do have limitations in that they do not
reflect certain items that may have a material impact on our
reported financial results. As such, these non-GAAP measures should
be viewed in conjunction with both our financial statements
prepared in accordance with GAAP and the reconciliation of the
supplemental non-GAAP financial measures to the comparable GAAP
results provided for the specific periods presented, which are
attached to this release.
Surmodics, Inc. and
Subsidiaries
Condensed Consolidated
Statements of Operations
(in thousands, except per share
data)
(Unaudited)
Three Months Ended March
31,
Six Months Ended March
31,
2024
2023
2024
2023
Revenue:
Product sales
$
18,099
$
15,350
$
36,926
$
29,584
Royalties and license fees
11,411
9,429
20,590
18,194
Research, development and other
2,448
2,419
4,994
4,353
Total revenue
31,958
27,198
62,510
52,131
Operating costs and expenses:
Product costs
7,101
5,738
15,904
11,005
Research and development
10,229
12,924
18,893
25,667
Selling, general and administrative
13,093
12,970
25,630
26,209
Acquired intangible asset amortization
876
867
1,746
1,780
Restructuring expense
—
1,282
—
1,282
Total operating costs and expenses
31,299
33,781
62,173
65,943
Operating income (loss)
659
(6,583
)
337
(13,812
)
Other expense, net
(493
)
(782
)
(895
)
(1,561
)
Income (loss) before income taxes
166
(7,365
)
(558
)
(15,373
)
Income tax benefit (expense)
81
(368
)
19
(203
)
Net income (loss)
$
247
$
(7,733
)
$
(539
)
$
(15,576
)
Basic net income (loss) per share
$
0.02
$
(0.55
)
$
(0.04
)
$
(1.11
)
Diluted net income (loss) per share
$
0.02
$
(0.55
)
$
(0.04
)
$
(1.11
)
Weighted average number of shares
outstanding:
Basic
14,152
14,030
14,127
14,010
Diluted
14,182
14,030
14,127
14,010
Surmodics, Inc. and
Subsidiaries
Condensed Consolidated Balance
Sheets
(in thousands)
March 31,
September 30,
2024
2023
Assets
(Unaudited)
(See Note)
Current Assets:
Cash and cash equivalents
$
33,030
$
41,419
Available-for-sale securities
7,909
3,933
Accounts receivable, net
12,319
10,850
Contract assets
10,650
7,796
Inventories
15,405
14,839
Prepaids and other
4,950
7,854
Total Current Assets
84,263
86,691
Property and equipment, net
25,718
26,026
Intangible assets, net
24,784
26,206
Goodwill
43,576
42,946
Other assets
4,464
3,864
Total Assets
$
182,805
$
185,733
Liabilities and Stockholders’
Equity
Current Liabilities:
Deferred revenue
4,749
4,378
Other current liabilities
14,448
19,576
Total Current Liabilities
19,197
23,954
Long-term debt, net
29,480
29,405
Deferred revenue
—
2,400
Other long-term liabilities
10,178
10,064
Total Liabilities
58,855
65,823
Total Stockholders’ Equity
123,950
119,910
Total Liabilities and Stockholders’
Equity
$
182,805
$
185,733
Note: Derived from audited financial
statements as of the date indicated.
Surmodics, Inc. and
Subsidiaries
Condensed Consolidated
Statements of Cash Flows
(in thousands)
(Unaudited)
Six Months Ended March
31,
2024
2023
Operating Activities:
Net loss
$
(539
)
$
(15,576
)
Adjustments to reconcile net loss to net
cash used in operating activities:
Depreciation and amortization
4,429
4,214
Stock-based compensation
4,094
3,747
Deferred taxes
(189
)
(217
)
Other
300
730
Change in operating assets and
liabilities:
Accounts receivable and contract
assets
(4,337
)
(2,346
)
Inventories
(565
)
(1,948
)
Prepaids and other
2,740
(1,582
)
Accounts payable
4
279
Accrued liabilities
(5,007
)
(4,064
)
Income taxes
(279
)
2,629
Deferred revenue
(2,028
)
(2,493
)
Net cash used in operating activities
(1,377
)
(16,627
)
Investing Activities:
Purchases of property and equipment
(1,991
)
(1,700
)
Purchases of available-for-sale
securities
(13,682
)
—
Maturities of available-for-sale
securities
10,000
—
Net cash used in investing activities
(5,673
)
(1,700
)
Financing Activities:
Payments of short-term borrowings
—
(10,000
)
Proceeds from issuance of long-term
debt
—
29,664
Payments of debt issuance costs
—
(611
)
Issuance of common stock
570
803
Payments for taxes related to net share
settlement of equity awards
(1,093
)
(872
)
Payments for acquisition of in-process
research and development
(931
)
(978
)
Net cash (used in) provided by financing
activities
(1,454
)
18,006
Effect of exchange rate changes on
cash
115
503
Net change in cash and cash
equivalents
(8,389
)
182
Cash and Cash Equivalents:
Beginning of period
41,419
18,998
End of period
$
33,030
$
19,180
Surmodics, Inc. and
Subsidiaries
Supplemental Revenue
Information
(in thousands)
(Unaudited)
Three Months Ended March
31,
Increase (Decrease)
2024
2023
$
%
Medical Device Revenue
Product sales
$
11,100
$
7,914
$
3,186
40
%
Royalties & license fees – performance
coatings
10,323
8,098
2,225
27
%
License fees – SurVeil DCB(1)
1,088
1,331
(243
)
(18
)%
R&D and other
2,315
2,364
(49
)
(2
)%
Medical Device revenue
24,826
19,707
5,119
26
%
In Vitro Diagnostics Revenue
Product sales
6,999
7,436
(437
)
(6
)%
R&D and other
133
55
78
142
%
In Vitro Diagnostics revenue
7,132
7,491
(359
)
(5
)%
Total Revenue
$
31,958
$
27,198
$
4,760
18
%
Medical Device Revenue, excluding
SurVeil DCB license fees(1)
$
23,738
$
18,376
$
5,362
29
%
Total Revenue, excluding SurVeil DCB
license fees(1)
$
30,870
$
25,867
$
5,003
19
%
Six Months Ended March
31,
Increase (Decrease)
2024
2023
$
%
Medical Device Revenue
Product sales
$
23,050
$
16,294
$
6,756
41
%
Royalties & license fees – performance
coatings
18,531
15,567
2,964
19
%
License fees – SurVeil DCB(1)
2,059
2,627
(568
)
(22
)%
R&D and other
4,731
4,237
494
12
%
Medical Device revenue
48,371
38,725
9,646
25
%
In Vitro Diagnostics Revenue
Product sales
13,876
13,290
586
4
%
R&D and other
263
116
147
127
%
In Vitro Diagnostics revenue
14,139
13,406
733
5
%
Total Revenue
$
62,510
$
52,131
$
10,379
20
%
Medical Device Revenue, excluding
SurVeil DCB license fees(1)
$
46,312
$
36,098
$
10,214
28
%
Total Revenue, excluding SurVeil DCB
license fees(1)
$
60,451
$
49,504
$
10,947
22
%
Surmodics, Inc. and
Subsidiaries
Supplemental Segment
Information
(in thousands)
(Unaudited)
Three Months Ended March
31,
Increase (Decrease)
2024
2023
$
Operating Income (Loss):
Medical Device
$
302
$
(7,059
)
$
7,361
In Vitro Diagnostics
3,356
3,636
(280
)
Total segment operating income (loss)
3,658
(3,423
)
7,081
Corporate
(2,999
)
(3,160
)
161
Total Operating Income (Loss)
$
659
$
(6,583
)
$
7,242
Six Months Ended March
31,
Increase (Decrease)
2024
2023
$
Operating Income (Loss):
Medical Device
$
78
$
(14,294
)
$
14,372
In Vitro Diagnostics
6,480
6,584
(104
)
Total segment operating income (loss)
6,558
(7,710
)
14,268
Corporate
(6,221
)
(6,102
)
(119
)
Total Operating Income (Loss)
$
337
$
(13,812
)
$
14,149
Surmodics, Inc. and
Subsidiaries
GAAP to Non-GAAP
Reconciliation: EBITDA and Adjusted EBITDA
(in thousands)
(Unaudited)
Three Months Ended March
31,
Increase (Decrease)
2024
2023
$
Net income (loss)
$
247
$
(7,733
)
$
7,980
Income tax (benefit) expense
(81
)
368
(449
)
Depreciation and amortization
2,096
2,092
4
Interest expense, net
881
884
(3
)
Investment income, net
(460
)
(177
)
(283
)
EBITDA
2,683
(4,566
)
7,249
Adjustments:
Stock-based compensation expense
2,126
1,782
344
Restructuring expense(5)
—
1,282
(1,282
)
Adjusted EBITDA
$
4,809
$
(1,502
)
$
6,311
Six Months Ended March
31,
Increase (Decrease)
2024
2023
$
Net loss
$
(539
)
$
(15,576
)
$
15,037
Income tax (benefit) expense
(19
)
203
(222
)
Depreciation and amortization
4,429
4,214
215
Interest expense, net
1,777
1,710
67
Investment income, net
(999
)
(349
)
(650
)
EBITDA
4,649
(9,798
)
14,447
Adjustments:
Stock-based compensation expense
4,094
3,747
347
Restructuring expense(5)
—
1,282
(1,282
)
Adjusted EBITDA
$
8,743
$
(4,769
)
$
13,512
Surmodics, Inc. and
Subsidiaries
GAAP to Non-GAAP
Reconciliation: Net Income (Loss) and Diluted EPS
(in thousands, except per share
data)
(Unaudited)
Three Months Ended March 31,
2024
Operating Income
Income Before
Income Taxes
Net Income(7)
Diluted EPS
GAAP
$
659
2.1
%
$
166
$
247
$
0.02
Adjustments:
Amortization of acquired intangible
assets(6)
876
2.7
%
876
810
0.05
Non-GAAP
$
1,535
4.8
%
$
1,042
$
1,057
$
0.07
Diluted weighted average shares
outstanding(8)
14,182
Three Months Ended March 31,
2023
Operating Loss
Loss Before
Income Taxes
Net Loss(7)
Diluted EPS
GAAP
$
(6,583
)
(24.2
)%
$
(7,365
)
$
(7,733
)
$
(0.55
)
Adjustments:
Amortization of acquired intangible
assets(6)
867
3.2
%
867
802
0.06
Restructuring expense(5)
1,282
4.7
%
1,282
1,282
0.09
Non-GAAP
$
(4,434
)
(16.3
)%
$
(5,216
)
$
(5,649
)
$
(0.40
)
Diluted weighted average shares
outstanding(8)
14,030
Six Months Ended March 31,
2024
Operating Income
(Loss) Income
Before Income
Taxes
Net (Loss) Income(7)
Diluted EPS
GAAP
$
337
0.5
%
$
(558
)
$
(539
)
$
(0.04
)
Adjustments:
Amortization of acquired intangible
assets(6)
1,746
2.8
%
1,746
1,615
0.12
Non-GAAP
$
2,083
3.3
%
$
1,188
$
1,076
$
0.08
Diluted weighted average shares
outstanding(8)
14,172
Six Months Ended March 31,
2023
Operating Loss
Loss Before
Income Taxes
Net Loss(7)
Diluted EPS
GAAP
$
(13,812
)
(26.5
)%
$
(15,373
)
$
(15,576
)
$
(1.11
)
Adjustments:
Amortization of acquired intangible
assets(6)
1,780
3.4
%
1,780
1,654
0.12
Restructuring expense(5)
1,282
2.5
%
1,282
1,282
0.09
Non-GAAP
$
(10,750
)
(20.6
)%
$
(12,311
)
$
(12,640
)
$
(0.90
)
Diluted weighted average shares
outstanding(8)
14,010
Surmodics, Inc. and
Subsidiaries
Guidance Reconciliation:
Revenue
For the Fiscal Year Ending
September 30, 2024
(in millions)
(Unaudited)
Fiscal 2024 Full-Year
Estimate
Increase (Decrease)
Low
High
Low
High
Fiscal 2023
Total Revenue
$
122
$
124
(8
)%
(6
)%
$
133
License fees – SurVeil DCB(1)
(4
)
(4
)
(86
)%
(86
)%
(30
)
Total Revenue, excluding SurVeil DCB
license fees(1)
$
118
$
120
15
%
17
%
$
103
Surmodics, Inc. and
Subsidiaries
Guidance Reconciliation:
Non-GAAP Diluted EPS
For the Fiscal Year Ending
September 30, 2024
(shares in thousands)
(Unaudited)
Fiscal 2024 Full-Year
Estimate
Low
High
GAAP Diluted EPS
$
(0.90
)
$
(0.70
)
Amortization of acquired intangibles per
diluted share(5)
0.23
0.23
Non-GAAP Diluted EPS
$
(0.67
)
$
(0.47
)
Diluted weighted average shares
outstanding
14,150
(1)
SurVeil DCB license fee revenue represents
revenue recognition on milestone payments received under the
company’s Development and Distribution Agreement with Abbott
(“Abbott Agreement”). For further details, refer to Supplemental Revenue Information and Guidance Reconciliation: Revenue.
(2)
For the calculation of Adjusted EBITDA,
refer to GAAP to Non-GAAP Reconciliation:
EBITDA and Adjusted EBITDA.
(3)
Product gross profit equals product sales
less product costs, as reported on the condensed consolidated
statements of operations. Product gross margin equals product gross
profit as a percentage of product sales.
(4)
For the calculation of Non-GAAP net income
(loss) and Non-GAAP income (loss) per diluted share (also referred
to as Non-GAAP diluted EPS), refer to GAAP to
Non-GAAP Reconciliation: Net Income (Loss) and Diluted EPS
and Guidance Reconciliation: Non-GAAP Diluted
EPS.
(5)
Restructuring expense consists of
severance and related costs specifically associated with a
workforce restructuring implemented in the second quarter of fiscal
2023.
(6)
Represents amortization of business
acquisition-related intangible assets and associated tax impact. A
significant portion of the business acquisition-related
amortization is not tax deductible.
(7)
Net income (loss) includes the effect of
GAAP to Non-GAAP adjustments on income tax benefit (expense),
taking into account deferred taxes net of valuation allowances, as
well as non-deductible items. Income tax impacts were estimated
using the applicable statutory rate (21% in the U.S. and 12.5% in
Ireland).
(8)
Diluted weighted average shares
outstanding used in the calculation of EPS was the same for GAAP
EPS and Non-GAAP EPS for the three months ended March 31, 2024 and
2023 and the six months ended March 31, 2023. For the six months
ended March 31, 2024, diluted weighted average shares outstanding
used in the calculation of EPS was 14,127 for GAAP EPS due to the
GAAP net loss in the period and was 14,172 for Non-GAAP EPS
corresponding to the Non-GAAP net income in the period.
(9)
Surmodics data on file.
(10)
Gray BH, Wheibe E, Dicks AB, Low ML,
Tingen JS. Pounce Thrombectomy System to Treat Acute and Chronic
Peripheral Arterial Occlusions. Ann Vasc Surg. 2023;96:104-114.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240501143641/en/
Surmodics Investor Inquiries Jack Powell, Investor Relations
ir@surmodics.com
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