Omega Silicone, Inc.

Omega Silicone, Inc. — FDA 510(k) Submissions

Omega Silicone, Inc. has submitted 5 FDA 510(k) premarket notifications since 1987, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Chin, Internal, Appliance, Facial Fracture, External, Prosthesis, Nose, Internal, Button, Nasal Septal . Use the specialty filter in the sidebar to narrow results.