As the medical device industry continues to expand, intellectual property (IP) considerations — especially those concerning ...

AirLife and Vyaire are recalling specific infant breathing support systems due to a potentially dangerous defect that could ...

Using recalled AirLife Infant Heated Wire Circuits could cause cause carbon dioxide build up in the blood, a lack of oxygen in the body, organ failure or death, according to the FDA.

Synchrony Medical announced that it received FDA 510 (k) clearance for its LibAirty airway clearance system.

Globally, generative artificial intelligence (Gen AI) and agentic AI are increasingly being integrated into medical devices, transforming both clinical workflows and patient care. Gen AI is primarily ...

"FDA approves Dymicron’s study of cervical artificial disc" was originally created and published by Medical Device Network, a ...

New Technological Processes and FDA Approvals Highlight AI and IoT Integration" BOSTON, July 10, 2025 /PRNewswire/ -- According to the latest ...

U.S. physicians are losing trust in the FDA and CDC, presenting a new challenge — and opportunity — for device developers and ...

Dymicron's Triadyme-C achieves critical milestone to begin U.S. IDE clinical trial OREM, Utah, July 10, 2025 /PRNewswire/ -- ...

Pioneering a new category of robotics in healthcare, Mendaera’s Focalist™ System, cleared for precise instrument placement ...

Medical device recalls are essential to patient safety, addressing critical issues in devices that may pose health risks. Here are some of the latest recalls reported to the FDA: Airlife and Vyaire ...