Hgm, Inc.

Hgm, Inc. — FDA 510(k) Submissions

Hgm, Inc. has submitted 23 FDA 510(k) premarket notifications since 1983, of which 23 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Laser Surgical Instrument, Laser, Ophthalmic, Laser For Gastro-urology Use, Transilluminator, Ac-powered, Laser, Surgical, Gynecologic . Use the specialty filter in the sidebar to narrow results.