Numed Technologies, Inc.

Numed Technologies, Inc. — FDA 510(k) Submissions

Numed Technologies, Inc. has submitted 5 FDA 510(k) premarket notifications since 1992, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, Gynecologic (and Accessories), Laparoscope, General & Plastic Surgery, Coagulator, Culdoscopic (and Accessories) . Use the specialty filter in the sidebar to narrow results.