Form 6-K - Report of foreign issuer [Rules 13a-16 and 15d-16]
04 Marzo 2024 - 3:25PM
Edgar (US Regulatory)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 6-K
REPORT OF FOREIGN PRIVATE ISSUER
PURSUANT TO RULE 13a-16 OR 15d-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934
For the Month of March 2024
Commission File Number: 001-40303
Inspira Technologies Oxy B.H.N. Ltd.
(Translation of registrant’s name into
English)
2 Ha-Tidhar St.
Ra’anana 4366504, Israel
(Address of principal executive office)
Indicate by check mark whether the registrant
files or will file annual reports under cover of Form 20-F or Form 40-F:
☒ Form 20-F ☐ Form
40-F
CONTENTS
On March 4, 2024, Inspira
Technologies Oxy B.H.N. Ltd., or the Registrant, issued a press release titled “Inspira™ Announces Plans to Report the Primary
Results for a Core Blood Oxygenation Technology Within Days,” a copy of which is furnished as Exhibit 99.1 with this report of foreign
private issuer on Form 6-K.
The
first, third, fourth and fifth paragraphs and the section titled “Forward-Looking Statements” in the press release are incorporated
by reference into the Registrant’s Registration Statements on Form F-3 (Registration No. 333-266748)
and Form S-8 (Registration No. 333-259057), filed with the Securities and Exchange Commission, to be a part thereof from the date
on which this report is submitted, to the extent not superseded by documents or reports subsequently filed or furnished.
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.
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Inspira Technologies Oxy B.H.N. Ltd. |
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Date: March 4, 2024 |
By: |
/s/ Dagi Ben-Noon |
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Name: |
Dagi Ben-Noon |
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Title: |
Chief Executive Officer |
Exhibit 99.1
Inspira™ Announces Plans to Report the Primary Results for
a Core Blood Oxygenation Technology Within Days
| ● | The major milestone refers to Inspira’s proprietary technology to oxygenate
blood for the INSPIRA™ ART (Gen 2). This patented tech is considered by Inspira to be a game-changer and also aims to replace technologies
used today by current medical device companies. |
| ● | Anticipated U.S. Food and Drug Administration (FDA) Clearance for INSPIRA™
ART100 (Gen 1) in the first half of 2024, to address the $1.16 Billion perfusion systems market. |
Ra’anana, Israel, March 04, 2024 (GLOBE
NEWSWIRE) -- Inspira™ Technologies OXY B.H.N. Ltd. (Nasdaq: IINN, IINNW) (the “Company” or “Inspira”),
a breakthrough medical technology company, announced today that the Company’s President, and co-founder, Mr. Joe Hayon, presented
key highlights included in the Company’s Investor Presentation and announced the Company’s next major milestone of a core
blood oxygenation technology of the INSPIRA ART (Gen 2). The INSPIRA ART (Gen 2) is designed to utilize adaptive oxygenation technology,
leveraging the proprietary HYLA™ blood Sensor and VORTX™ Orbiting Blood Oxygenation, to delivery oxygen straight into the
blood. The proprietary core technology has undergone a series of testing in a variety of settings, with the results being collected and
analyzed. The results refer to the INSPIRA ART (Gen 2), with the new core technology potentially being suitable for replacing current
solutions in medical markets dominated by leading medical device companies. The Company plans to announce the primary results around
the core blood oxygenation technology of the INSPIRA ART (Gen 2) within days.
Mr. Hayon shared “We have an appetite to revolutionize the huge
life-support mechanical ventilation market. In addition, it’s important to emphasize that we believe INSPIRA ART100 (Gen 1) itself
addresses $1B market.” Key highlights from the conference call included:
| ● | The current healthcare challenge and a personal story. |
| ● | The solution – Inspira’s oxygen delivery straight into the blood. |
| ● | INSPIRA™ ART (Gen 2), Adaptive Blood Oxygenation and expected major
milestone. |
| ● | INSPIRA™ ART Gen 1 and Gen 2 product overview. |
| ● | Anticipated FDA Clearance for INSPIRA™ ART100 (Gen 1). |
Mr. Hayon shared a heartfelt personal story and the profound impact
of Inspira beyond technological innovation. He recounted his father’s prolonged reliance on mechanical ventilation, painting a vivid picture
of the challenges and complications associated with traditional ventilation methods. Through conversations with critical care physicians,
the necessity for Inspira’s technology became clear – a sentiment echoed by medical professionals eager to integrate INSPIRA ART
into clinical practice.
Emphasizing the Company’s core mission, Mr. Hayon continued to share
how Inspira is focused on delivering oxygen straight into the blood. The Company is advancing two generations of blood oxygenation solutions.
INSPIRA ART100 (Gen 1), designed to perform blood oxygenation as a cardio-pulmonary bypass device, is anticipated to be cleared by the
FDA in the first half of 2024. With the planned FDA submission and clearance of the HYLA, the INSPIRA ART100 is then intended to be integrated
with blood monitoring technologies from the HYLA. In parallel, the Company is rapidly developing the INSPIRA ART (Gen 2), designed to
perform adaptive blood oxygenation, embedded with the HYLA advanced continuous blood monitoring, to provide real-time detection of changes
and provide decision-making assistance data and the VORTX orbiting blood oxygenation delivery system.
We believe that since the blood holds so many secrets about patient
condition and response to treatment, the collection, aggregation and analysis of data by the INSPIRA ART will potentially open a huge
market opportunity for the Company, as we aim to revolutionize the treatment of patients while they are awake and without the need for
mechanical ventilation. The forthcoming expected FDA clearance of the INSPIRA ART100 will mark a pivotal achievement, which we believe
will reinforce Inspira’s position as a disruptive force in the medical landscape.
Inspira Technologies OXY B.H.N. Ltd.
Inspira™ Technologies is an innovative medical technology company
in the respiratory treatment arena. The Company has developed a breakthrough Augmented Respiration Technology (INSPIRA ART), designed
to rebalance patient oxygen saturation levels. This technology potentially allows patients to remain awake during treatment while reducing
the need for highly invasive, risky, and costly mechanical ventilation systems that require intubation and medically induced coma. The
Company’s products have not yet been tested or used in humans and has not been approved by any regulatory entity.
For more information, please visit our corporate website: https://inspira-technologies.com
Forward-Looking Statement Disclaimer
This press release contains express or implied forward-looking statements
pursuant to U.S. Federal securities laws. These forward-looking statements and their implications are based on the current expectations
of the management of the Company only and are subject to a number of factors and uncertainties that could cause actual results to differ
materially from those described in the forward-looking statements. For example, the Company is using forward-looking statements when it
discusses the potential benefits of the Company’s products and potential products, the potential addressable market for its products,
that it intends to announce the primary results for its core blood oxygenation technology within days, the expected timing of FDA approval
and the intended future submission of products for FDA approval, the belief that the INSPIRA ART will potentially open a huge market opportunity
and that the expected FDA clearance of the INSPIRA ART100 will mark a pivotal achievement, which it believes will reinforce its position
as a disruptive force in the medical landscape. These forward-looking statements and their implications are based solely on the current
expectations of the Company’s management and are subject to a number of factors and uncertainties that could cause actual results
to differ materially from those described in the forward-looking statements. Except as otherwise required by law, the Company undertakes
no obligation to publicly release any revisions to these forward-looking statements to reflect events or circumstances after the date
hereof or to reflect the occurrence of unanticipated events. More detailed information about the risks and uncertainties affecting the
Company is contained under the heading “Risk Factors” in the Company’s annual report on Form 20-F for the fiscal year
ended December 31, 2022 filed with the U.S. Securities and Exchange Commission (the “SEC”), which is available on the SEC’s
website, www.sec.gov
For more details:
Public Relations Manager
Adi Shmueli
Inspira Technologies
info@inspirao2.com
+972-9-9664485
MRK-ARS-091
Copyright © 2018-2024 Inspira Technologies OXY B.H.N. LTD., All
rights reserved.
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