Allergan, Inc.

Allergan, Inc. — FDA 510(k) Submissions

Allergan, Inc. has submitted 33 FDA 510(k) premarket notifications since 1982, of which 33 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accessories, Soft Lens Products, Lens, Contact (polymethylmethacrylate), Unit, Phacofragmentation, Keratome, Ac-powered, Amplifier, Physiological Signal . Use the specialty filter in the sidebar to narrow results.