Gemore Technology Co, Ltd.

Gemore Technology Co, Ltd. — FDA 510(k) Submissions

Gemore Technology Co, Ltd. has submitted 14 FDA 510(k) premarket notifications since 2003, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Nerve, Transcutaneous, For Pain Relief, Stimulator, Nerve, Transcutaneous, Over-the-counter, Stimulator, Muscle, Powered, For Muscle Conditioning, Interferential Current Therapy, Electrode, Cutaneous . Use the specialty filter in the sidebar to narrow results.