Significant progress in HYLA blood sensor and INSPIRA ART core technologies RA'ANANA, Israel, March 11, 2025 /PRNewswire/ -- Inspira Technologies OXY B.H.N. Ltd.

Inspira's AI-powered continuous blood monitoring technology demonstrated a high degree of accuracy in a key parameter, targeting multiple multi-billion-dollar market ...

FOR IMMEDIATE RELEASESpineart and eCential Roboticsannounce FDA clearance of PERLA® App for use with Op.nTM robotic navigation platformDallas, ...

The US Food and Drug Administration (FDA) has cleared Miach Orthopaedics Bridge-Enhanced ACL Restoration (BEAR) implant for expanded use in treating complete and partial anterior cruciate ligament ...

The US Food and Drug Administration (FDA) has granted clearance to Qiagen’s QIAstat-Dx Gastrointestinal Panel 2 Mini B, expanding the company’s syndromic testing offerings in the US.

With the FDA’s recent emphasis on cybersecurity as a critical component of medical device and software safety, obtaining clearance is more vital than ever. The latest enhancements to the ...

The pulse detection featured received clearance from the U.S. FDA on Feb. 26 and Google plans to make it available on its Pixel Watch 3 starting in March. Pulse detection is already available for ...

The U.S. FDA hasn’t taken up criminal justice as a sideline, but it did just clear Sonio Suspect. Far from a social miscreant, Suspect improves detection of fetal anomalies by 22 points by ...

On January 17, 2025, the US FDA cleared the Inmedix CloudHRV System for US commercialization. Its intended use is as a heart rate variability (HRV) diagnostic to be applied in the clinical setting ...