The rise of AI in health care presents new challenges related to the patentability and regulation of AI-driven medical ...

nbsp, Medical devices are divided into three categories: Class I, II and III relating to their properties, uses and potential risk to the user. In broad terms Class I devices (those under routine ...

RICHMOND, Texas, April 10, 2025 /PRNewswire/ -- Velentium, a leading engineering and manufacturing firm specializing in the design and development of Class II and Class III medical devices, is ...

——The World's First Precisely Regulated Injectable CaHA Filler, Accelerating Compliance in the Medical Aesthetics Industry in China. Calcium hydroxylapatite (CaHA) microspheres have become a ...

Certain devices considered not to have undergone full review – such as, for example, Class IIb (non-well established technology) implantable and Class III medical devices approved via a route ...

Q'Apel has submitted three Medical Device Reportable events for the Hippo product to date; these adverse events include a reported tip detachment, retrieved without patient injury; a vessel ...