Neurovalens , Ltd.

Neurovalens , Ltd. — FDA 510(k) Submissions

Neurovalens , Ltd. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cranial Electrotherapy Stimulator To Treat Insomnia And/or Anxiety . Use the specialty filter in the sidebar to narrow results.