Stimwave Technologies, Inc.

Stimwave Technologies, Inc. — FDA 510(k) Submissions

Stimwave Technologies, Inc. has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Spinal-cord, Implanted (pain Relief) . Use the specialty filter in the sidebar to narrow results.