The company completed a clinical trial at nine centers across the U.S., Europe and Asia before it received FDA approval.

The U.S. Medical Device 3PL market is set for growth, driven by the complexity of modern devices needing specialized ...

Vivos Inc. (OTCQB: RDGL), a pioneer in Precision Radionuclide TherapyTM (PRnT) solutions, today announced the submission of ...

Each year, choking claims the lives of more than 4,100 Americans who are 65 or older. It’s the most vulnerable age group, ...

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

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

The past six months at the US Department of Health and Human Services and the US Food and Drug Administration’s Center for Devices and ...

Using recalled AirLife Infant Heated Wire Circuits could cause cause carbon dioxide build up in the blood, a lack of oxygen ...

With clinical success demonstrated at Atlantic Health System, JFK University Medical Center, Mount Sinai Health System, St. Lukes Health System, and University of Virginia, Borvo EVAC meets the ...

Preceptis Medical's Hummingbird Tympanostomy Tube System can perform a myringotomy and insert an ear tube with only topical ...

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 ...