Medtronic wins CE mark for left atrial appendage exclusion system
October 1, 2025
Medtronic (NYSE: MDT)+
announced today that it received CE mark approval for its Penditure LAA exclusion system.
Medtronic (NYSE: MDT)+
announced today that it received CE mark approval for its Penditure LAA exclusion system.
NEW YORK, Sept. 30, 2025 /PRNewswire/ — Aidoc, the global leader in clinical AI, today announced the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation for the company’s novel multi-triage solution that flags a wide array of life-threatening, time-sensitive medical conditions, all within a single workflow. Built on CARE™, the first clinical-grade foundation model in healthcare with FDA cleared solutions, and deployed through Aidoc’s aiOS™ platform, the solution is designed to help care teams attend to high–risk cases faster and more consistently across the health system.
SAN FRANCISCO, Sept. 30, 2025 /PRNewswire/ — Avive Solutions, Inc. is proud to announce a significant advancement in public safety and emergency preparedness: the smallest, lightest AED on the market, the Avive Connect AED®, is safe and effective for use on aircrafts. Following rigorous testing and evaluation, this clearance confirms that the device is safe and effective for use on aircraft, enabling a new standard of emergency response at 30,000 feet.
Penn researchers have developed an AI-powered device that turns ordinary glasses into a smart, energy-efficient health monitor by watching you blink.
New research from the MRC Laboratory of Medical Sciences (LMS) provides a powerful, scalable method for finding treatments for rare genetic diseases using tiny, transparent worms.
Researchers at Oregon Health & Science University have accomplished a unique proof of concept to treat infertility by turning skin cells into eggs capable of producing early human embryos. The research is published in Nature Communications.
An advanced AI tool can detect tiny brain lesions that cause severe epilepsy in children, allowing faster diagnosis, more precise treatment and a potential cure, according to a new study.
Zenflow announced today that it received FDA 510(k) clearance for its Spring scope and camera control unit (CCU).
Outlook Surgical this week announced it received FDA 510(k) clearance for its Inova 1 Towerless Endoscope System.
Olympus announced today that it launched its Olysense platform with Caddie medical device software for early colorectal polyp detection.