Sorenson Laboratories, Inc.

Sorenson Laboratories, Inc. — FDA 510(k) Submissions

Sorenson Laboratories, Inc. has submitted 3 FDA 510(k) premarket notifications since 1992, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Laser Surgical Instrument, Apparatus, Exhaust, Surgical, Lens, Surgical, Laser, Accesssory, Ophthalmic Laser . Use the specialty filter in the sidebar to narrow results.