The Magstim Company Limited

The Magstim Company Limited — FDA 510(k) Submissions

The Magstim Company Limited has submitted 3 FDA 510(k) premarket notifications since 2024, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Transcranial Magnetic Stimulator, Electromagnetic Stimulator, Pain Relief . Use the specialty filter in the sidebar to narrow results.