Matrix Medica, Inc.

Matrix Medica, Inc. — FDA 510(k) Submissions

Matrix Medica, Inc. has submitted 14 FDA 510(k) premarket notifications since 1985, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Operative Dental, Dressing, Wound, Occlusive, Mixer, Breathing Gases, Anesthesia Inhalation, Gas-machine, Anesthesia, Tester, Defibrillator . Use the specialty filter in the sidebar to narrow results.