Maddak, Inc.

Maddak, Inc. — FDA 510(k) Submissions

Maddak, Inc. has submitted 51 FDA 510(k) premarket notifications since 1977, of which 51 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Exerciser, Non-measuring, Cane, Sling, Arm, Adaptor, Hygiene, Cushion, Flotation . Use the specialty filter in the sidebar to narrow results.