Woodlyn, Inc.

Woodlyn, Inc. — FDA 510(k) Submissions

Woodlyn, Inc. has submitted 19 FDA 510(k) premarket notifications since 1984, of which 19 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ophthalmoscope, Ac-powered, Set, Lens, Trial, Ophthalmic, Biomicroscope, Slit-lamp, Ac-powered, Tonometer, Ac-powered, Keratoscope, Ac-powered . Use the specialty filter in the sidebar to narrow results.