Orthion Corp.

Orthion Corp. — FDA 510(k) Submissions

Orthion Corp. has submitted 11 FDA 510(k) premarket notifications since 1981, of which 11 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Aid, Transfer, Adaptor, Hygiene, Sling, Arm, Overhead Supported, Stimulator, Muscle, Powered, System, Telethermographic, Infrared . Use the specialty filter in the sidebar to narrow results.