Weero Co., Ltd.

Weero Co., Ltd. — FDA 510(k) Submissions

Weero Co., Ltd. has submitted 4 FDA 510(k) premarket notifications since 2024, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Massager, Vacuum, Radio Frequency Induced Heat, Stimulator, Muscle, Powered . Use the specialty filter in the sidebar to narrow results.