Manamed, Inc.

Manamed, Inc. — FDA 510(k) Submissions

Manamed, Inc. has submitted 7 FDA 510(k) premarket notifications since 2016, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Sleeve, Limb, Compressible, Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat, Massager, Powered Inflatable Tube, Stimulator, Nerve, Transcutaneous, Over-the-counter . Use the specialty filter in the sidebar to narrow results.