MONTVALE, N.J., Dec. 10, 2024 /PRNewswire/ — PENTAX Medical, a division of HOYA Group, has obtained US FDA 510(k) clearance for new models of the PENTAX Medical i20c Video Endoscope Series—PENTAX Medical Video Colonoscope EC34-i20cL, PENTAX Medical Video Upper GI Scope EG27‑i20c and Right/Left Wheel Extender OE-B17.

This doesn’t look like a typical blood pressure monitor – but that is exactly what it is.

Artivion (NYSE:AORT) this week announced it received FDA humanitarian device exemption (HDE) for its AMDS hybrid prosthesis.

EndoQuest Robotics announced today that it received FDA investigational device exemption (IDE) for a study of its surgical robot.