MALVERN, Pa., Nov. 11, 2024 (GLOBE NEWSWIRE) -- via IBN – Annovis Bio, Inc. (NYSE: ANVS) ('Annovis' or the 'Company'), a clinical-stage drug ...

Bayer has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its multi-patient Medrad Centargo computed tomography (CT) injection system. The injection system integrates with ...

Among those that voted "no", there were three who stated that if the FDA applied adequate special controls ... ProSense® system is marketed and sold worldwide for the indications cleared and approved ...

Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first ...

BOSTON, Nov. 6, 2024 /PRNewswire/ -- Zeta Surgical announced today that its Zeta Navigation System has received 510 (k) ...

Clearance for the Phase II oncology trial was achieved following productive feedback sessions with the FDA over the past few months and the submission of a final study protocol to the FDA in September ...

Alimetry has raised an oversubscribed US $18m A2 financing round to commercialize its wearable gut health monitoring device, ...

FDA regulations categorize medical devices into three classes, with varying levels of control to manage risks and ensure the safety of medical technologies.

Trump vows to let RFK Jr., who has called federal agencies “sock puppets” for industry interests, "go wild" on health, food and medicines.

Think of it as an Rx for your skin. “This is an FDA-cleared device that contains both 100 red and 62 blue LED lights for a full face light emitting treatment,” Gloria Lin, MD, board-certified ...