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 December 2024 (Report No. 3)
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 December 16, 2024, Inspira
Technologies Oxy B.H.N. Ltd., or the Registrant, issued a press release titled “Inspira™ Technologies Delivers Systems to
Leading Distributor for U.S. Deployment,” a copy of which is furnished as Exhibit 99.1 with this report of foreign private issuer
on Form 6-K.
The first three 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 Nos. 333-259057
and 333-277980),
filed with the Securities and Exchange Commission, to be a part thereof from the date on which this Report of Foreign Private Issuer on
Form 6-K is submitted, to the extent not superseded by documents or reports subsequently filed or furnished.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: December 16, 2024 |
By: |
/s/ Dagi Ben-Noon |
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Name: |
Dagi Ben-Noon |
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Title: |
Chief Executive Officer |
2
Exhibit 99.1
Inspira™ Technologies Delivers
Systems to Leading Distributor for U.S. Deployment
RA’ANANA, Israel– December 16, 2024 – Inspira Technologies
Oxy B.H.N. Ltd. (NASDAQ: IINN, IINNW), (“Inspira Technologies,” “Inspira” or the “Company”), a
groundbreaking respiratory support technology company, announced the delivery of INSPIRA™
ART100 systems to its U.S. distributor, Glo-Med Networks Inc (“Glo-Med”). The systems were shipped in fulfilment of a purchase
order issued by Glo-Med to Inspira.
The delivered INSPIRA™
ART100 systems will be distributed to sales targets across hospitals on the U.S. east coast and distributed to a cardiothoracic surgery
division at a leading New York hospital, ranked among the top 15 percent of cardiothoracic programs in the U.S., with a view
to collaborating with such hospital. The Company believes that the delivery of the INSPIRA™
ART100 to the U.S. market serves the Company’s goal well to introduce physicians and perfusionists to Inspira’s technologies and brand
via initial deployments at leading hospitals.
Designed in collaboration with leading U.S. clinicians, the INSPIRA™
ART100 cardiopulmonary bypass system revolutionizes extracorporeal blood circulation by combining cutting-edge technology with intuitive
design to optimize patient care during crucial times. The INSPIRA™
ART100 is planned to be integrated with the HYLA™, a continuous
blood monitoring technology designed to potentially detect real-time changes in patient condition. The HYLA™
is undergoing clinical evaluations at Sheba Hospital, ranked the 9th in the world by Newsweek™, in patients undergoing
open-heart procedures, in preparation of the Company’s planned U.S. Food and Drug Administration (“FDA”) submission of the first
configuration of the HYLA™ in 2025.
Dagi Ben-Noon, CEO of Inspira Technologies stated: “We
see this as merely the first deployment step in Inspira’s quest to revolutionize acute respiratory care with our groundbreaking technology
and superior products that we believe will follow this initial distribution.”
Inspira™ Technologies OXY B.H.N. Ltd.
Inspira Technologies is an innovative medical technology company in
the life support and respiratory treatment arena. The Company has developed a breakthrough Augmented Respiration Technology (INSPIRA™
ART), a groundbreaking device poised to revolutionize the $19 billion mechanical ventilation market. With 20 million intensive
care unit patients with acute respiratory failure each year, many of whom rely on mechanical ventilators, the INSPIRA ART offers a potential
alternative by elevating and stabilizing decreasing oxygen saturation levels in minutes without a ventilators, with patient being awake
during treatment. The INSPIRA ART is being equipped with the HYLA™ blood sensor technology, a real-time continuous blood monitoring
technology, aiming to alert physicians of changes in a patient’s condition without the need for intermittent actual blood samples, and
potentially supporting physicians in making informed decisions.
The Company’s INSPIRA™ ART100 system has obtained
FDA 510(k) clearance for use in Cardiopulmonary Bypass procedures, along with the Israeli AMAR certification for both Extra-Corporeal
Membrane Oxygenation and Cardiopulmonary Bypass procedures.
The Company’s other products and technologies, including the INSPIRA
ART also known as the INSPIRA™ ART500 or Gen 2, the INSPIRA™ Cardi-ART portable modular device, VORTX orbiting Oxygen Delivery
System and HYLA™ blood sensor, are currently being designed and developed, and have not yet been tested or used in humans and have
not been approved by any regulatory entity.
For more information, please visit our corporate website: https://inspira-technologies.com
Forward-Looking Statements
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 prospective distribution lines for the INSPIRA™
ART100 systems, the belief that the delivery of the INSPIRA™
ART100 to the U.S. market serves the Company’s goal well to introduce physicians and perfusionists to Inspira’s technologies and brand
via initial deployments at leading hospitals, the benefits of the INSPIRA™ ART100 , its plan to combine the INSPIRA™
ART100 with the HYLA™, the expected timing of the planned
FDA submission of the first configuration of the HYLA™ , and that
its sees these distribution lines as the first deployment step in Inspira’s quest to revolutionize acute respiratory care with its groundbreaking technology
and superior products that may follow. 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, 2023 filed
with the U.S. Securities and Exchange Commission (the “SEC”), which is available on the SEC’s website, www.sec.gov.
Contact:
For more information, contact:
Inspira Technologies – Media Relations
Email: info@inspirao2.com
Phone: +972-9-9664485
MRK-ARS-125
Copyright © 2018-2024 Inspira Technologies OXY B.H.N. LTD., All
rights reserved.
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