Koken Mfg Company, Inc.

Koken Mfg Company, Inc. — FDA 510(k) Submissions

Koken Mfg Company, Inc. has submitted 5 FDA 510(k) premarket notifications since 1986, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Table, Operating-room, Ac-powered, Chair, Ophthalmic, Ac-powered . Use the specialty filter in the sidebar to narrow results.