Philips Respironics has updated use instructions for three bi-level positive airway pressure machines, according to a recall ...

Device lobbyists’ priorities contrasted with patient advocates, who sought an increase in user fees and more funds for ...

U.S. health regulators are warning doctors and patients about safety issues with two separate Boston Scientific heart devices ...

DUBLIN, Jan. 19, 2024 /PRNewswire/ -- The "US FDA Medical Device Recalls: Trend and Impact Analysis" report has been added to ResearchAndMarkets.com's offering. This study analyzes the latest US ...

Medical device lobbyists and lawmakers have united in recent months over legislation that would make it easier to bill ...

Osaka: Takeda has announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for HyHub and HyHub Duo, devices for patients 17 years of age and older that allow ...

The U.S. FDA has staked out a position on the use of per- and polyfluoroalkyl substances in medical devices, declaring that ...

US FDA approves SetPoint Medical’s novel neuroimmune modulation device, SetPoint System for rheumatoid arthritis: Valencia, California Saturday, August 2, 2025, 17:00 Hrs [IST] ...

This article explains why Latin Americas demographic diversity, cost profile, and accelerating digital health infrastructure ...

The FDA has approved a medical device that stimulates the vagus nerve for the treatment of moderate-to-severe rheumatoid ...