Ybrain, Inc.

Ybrain, Inc. — FDA 510(k) Submissions

Ybrain, Inc. has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Nerve, Electrical, Transcutaneous, For Migraine . Use the specialty filter in the sidebar to narrow results.