Inspira Technologies to showcase FDA-cleared ART100 system at AmSECT 2026, targeting clinical decision-makers in perfusion technology.
Quiver AI Summary
Inspira Technologies OXY B.H.N. Ltd. announced it will showcase its FDA-cleared INSPIRA™ ART100 system at the American Society of Extracorporeal Technology (AmSECT) 64th International Conference, taking place from March 25 to 29, 2026, in Austin, Texas. The event targets clinical decision-makers in perfusion and cardiac surgery, providing a strategic platform for Inspira to leverage its recent FDA clearance to promote immediate clinical integration of the ART100 for cardiopulmonary bypass procedures. The showcase at Glo-Med Networks Inc.'s booth signifies Inspira's transition from development to active sales and market presence. Global VP Sales Mike Hershkovitz emphasized the company's goal to gain market share and expand clinical partnerships in the U.S. The conference is a key venue for advancing the understanding of perfusion technology and patient care.
Potential Positives
- Inspira Technologies will showcase its FDA-cleared INSPIRA™ ART100 system at a major medical conference, targeting key clinical decision makers in cardiothoracic surgery.
- The showcase leverages the FDA clearance of the ART100, highlighting its readiness for immediate clinical integration in hospitals, which could lead to increased adoption.
- Participation in the AmSECT conference demonstrates an active commercial pipeline and the company’s commitment to moving beyond product development into tangible market engagement.
- The event is a critical component of Inspira's U.S. commercial strategy, indicating plans for expansion of clinical partnerships and distribution networks.
Potential Negatives
- The reliance on forward-looking statements without definitive timelines or guarantees may create uncertainty about the company's future performance and actual market integration of the ART100 system.
- The press release emphasizes the need for additional clinical partnerships and market visibility, indicating that the company may still be in a developmental phase rather than fully operational in the market.
FAQ
What is the INSPIRA™ ART100 system?
The INSPIRA™ ART100 system is an FDA-cleared medical device for cardiopulmonary bypass procedures.
When will the ART100 be showcased?
The ART100 will be showcased at the AmSECT International Conference from March 25–29, 2026, in Austin, Texas.
Who is the U.S. distributor for the ART100?
The U.S. distributor for the ART100 is Glo-Med Networks Inc.
How does the ART100 support clinical integration?
The ART100's FDA clearance validates its readiness for immediate clinical integration in cardiopulmonary procedures.
Where can I learn more about Inspira Technologies?
More information about Inspira Technologies can be found at their official website: https://inspira-technologies.com.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
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Full Release
RA'ANANA, Israel, Feb. 17, 2026 (GLOBE NEWSWIRE) -- Inspira™ Technologies OXY B.H.N. Ltd. (NASDAQ: IINN, IINNW) (“Inspira Technologies,” “Inspira,” or the “Company”), a pioneer in innovative life-support and diagnostic technologies, today announced a strategic commercial showcase of its U.S. Food and Drug Administration (“FDA”)-cleared INSPIRA™ ART100 system. The system will be featured at the American Society of Extracorporeal Technology (AmSECT) 64th International Conference, taking place March 25–29, 2026, in Austin, Texas, at the exhibition booth of its U.S. distributor, Glo-Med Networks Inc. (“Glo-Med”).
Key Commercial Highlights:
- Targeting Clinical Decision Makers: The ART100 will be positioned at AmSECT, the premier global venue for perfusionists and cardiac surgical teams who directly influence hospital purchasing decisions.
- Leveraging FDA Clearance: The showcase capitalizes on the ART100’s FDA 510(k) clearance (received in May 2024) to validate the system’s readiness for immediate clinical integration in cardiopulmonary bypass procedures.
- Active Distribution Channel: The presentation via Glo-Med demonstrates an active commercial pipeline, moving beyond development into sales execution and market visibility.
“We are moving fast to translate our FDA clearance into market share. Presenting the ART100 alongside Glo-Med at AmSECT allows us to engage directly with the decision-makers who drive hospital purchasing,” said Mike Hershkovitz, Global VP Sales at Inspira Technologies . “This event marks a key phase in our U.S. commercial strategy as we expand our clinical partnerships and distribution footprint.”
Commercial and Clinical Inquiries Perfusion leaders, hospital administrators, and industry partners interested in scheduling a meeting with Mr. Hershkovitz during the conference are invited to contact: [email protected] .
About the 64th AmSECT International Conference
The AmSECT International Conference is the definitive global event for perfusion technology. Taking place March 25–29, 2026, in Austin, Texas, the conference features cutting-edge medical technologies and expert-led sessions shaping the future of extracorporeal circulation and patient care.
About Inspira Technologies
Inspira Technologies is a commercial-stage medical device company specializing in advanced respiratory support and real-time blood monitoring solutions. The Company’s FDA-cleared INSPIRA™ ART100 system is approved for cardiopulmonary bypass in the U.S. and ECMO (Extracorporeal Membrane Oxygenation) procedures outside the U.S and serves as a foundation for the development of the INSPIRA ART500, a next-generation system designed to deliver oxygenation while patients remain awake and spontaneously breathing. Inspira Technologies is also advancing HYLA™, a proprietary blood sensor platform offering continuous, non-invasive monitoring. With multiple cleared products, a growing IP portfolio, and strategic streamlining of its operations, Inspira Technologies is increasingly positioned as an attractive platform within the life-support and MedTech landscape. For more information, visit:
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 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 benefits and advantages of the ART100 system, its active commercial pipeline, the move into sales execution and market visibility and that it is actively expanding its clinical partnerships and distribution footprint in the U.S.. 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, 2024, filed with the U.S. Securities and Exchange Commission (the “SEC”), which is available on the SEC's website at
www.sec.gov
.
Company Contact
Inspira Technologies
Email
: [email protected]
Phone: +972-9-9664485