Lysonix, Inc.

Lysonix, Inc. — FDA 510(k) Submissions

Lysonix, Inc. has submitted 5 FDA 510(k) premarket notifications since 1997, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Suction, Lipoplasty For Removal, Laparoscope, General & Plastic Surgery, Catheter, Irrigation, Pump, Portable, Aspiration (manual Or Powered) . Use the specialty filter in the sidebar to narrow results.