Stephens Instruments

Stephens Instruments — FDA 510(k) Submissions

Stephens Instruments has submitted 5 FDA 510(k) premarket notifications since 2002, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Specula, Ophthalmic, Scissors, Ophthalmic, Hook, Ophthalmic, Trephine, Manual, Ophthalmic, Forceps, Ophthalmic . Use the specialty filter in the sidebar to narrow results.