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Inspira TM Announces 510(k) FDA Submission of INSPIRA TM ART100 Towards Commercialization Management estimates FDA clearance within approximately 6 months Ra'anana, Israel

Key Takeaway: Inspira Technologies OXY BHN Ltd. has announced the submission of its cardio-pulmonary bypass device, INSPIRA ART 100, to the FDA for clearance via the 510(k) pathway. The company anticipates receiving approval within six months, targeting the first half of 2024. This innovative device aims to reduce reliance on mechanical ventilation and aims to transform external breathing assistance for millions of patients requiring ventilation each year. Inspira plans to prepare for global deployment of its systems following FDA clearance.

Market Sentiment Analysis

POSITIVE FACTORS

  • Inspira Technologies submitted its INSPIRA ART 100 to the FDA, indicating progress towards commercialization.
  • The expected FDA clearance within approximately six months showcases optimism for its market introduction.
  • The technology aims to transform respiratory care, potentially benefiting over 20 million patients annually.

Full Press Release Details

Announces 510(k) FDA Submission of INSPIRATM ART100 Towards Commercialization
estimates FDA clearance within approximately 6 months
Israel, September 13, 2023 - Inspira Technologies OXY BHN Ltd. (Nasdaq: IINN, IINNW) (the "Company" or
"Inspira Technologies"), a company aiming to bring a paradigm shift to acute respiratory care by empowering breathing without
lungs, announced it had submitted its INSPIRA ART 100, a cardio-pulmonary bypass device, to the U.S. Food and Drug Administration (FDA)
via the 510(k) pathway, with potential clearance expected during the first half of 2024.
vision is to transform external breathing assistance for over 20 million patients each year that require ventilation and oxygenation
via external mechanical ventilation machinery. Legacy systems for breathing assistance are causing multiple complications leading to
physical damage, infection and possible death. Inspira aims to revolutionize the medical ventilation and oxygenation market by delivering
next-generation superior treatment, that will reduce the reliance on mechanical ventilation.
ART 100 was submitted today to the FDA post the completion of a comprehensive usability study in Boston, Massachusetts, with an expected
approval timeline of approximately six months, which is targeted for the first half of 2024.
Ben-Noon, CEO of Inspira, stated that,
are preparing for global deployments of our INSPIRA ART100 systems once FDA clearance is achieved.
future systems can save millions of lives and change external respiratory aid for over 20 million people each year. We aim to be a part
of this market over the next 5 years and are moving aggressively to achieve these goals."
Inspira Technologies OXY BHN Ltd.
Inspira Technologies maintains a steadfast mission to revolutionize acute respiratory care through innovation. The Company's primary
objective is the development of medical technologies and products aimed at preventing the necessity of mechanical ventilation. Its flagship
product, the INSPIRATM ART500, is intricately designed to rapidly elevate blood oxygen saturation levels, all while keeping
patients conscious and alert. Moreover, the Company is dedicated to providing advanced blood circulation technology and integrating AI-driven
monitoring and analytics. These elements combine to create patient-centric, data-driven solutions, ultimately enhancing patient outcomes
and optimizing hospital efficiency.
more information, please visit: https://inspira-technologies.com.
Forward-Looking Statement
This press release contains
express or implied forward-looking statements pursuant to US Federal securities laws. These forward-looking statements and their implications
are based on the current expectations of the management of the Company only. They are subject to several factors and uncertainties that
could cause actual results to differ materially from those described in the forward-looking statements. For example, the Company uses
forward-looking statements when discussing the expected timing of the clearance of the INSPIRA ART 100 by the FDA, that it is preparing
to globally deploy its product once the FDA clearance is obtained and the potential benefits of its products. 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 US Securities and Exchange Commission (the "SEC"),
which is available on the SEC's website, www.sec.gov.
Public Relations Manager
Inspira Technologies

Frequently Asked Questions

What is the INSPIRA ART 100?

The INSPIRA ART 100 is a cardio-pulmonary bypass device designed to assist breathing.

When is FDA clearance expected for ART 100?

FDA clearance for the INSPIRA ART 100 is anticipated within approximately six months.

How does Inspira Technologies aim to innovate respiratory care?

Inspira Technologies focuses on transforming respiratory care by reducing reliance on mechanical ventilation.

What is Inspira's long-term vision for its products?

Inspira aims to positively impact over 20 million patients needing external breathing assistance annually.

What other technologies does Inspira offer?

Inspira's flagship product, the ART500, enhances blood oxygen saturation while keeping patients alert.

Last updated: Sep 13, 2023