Medical Device Manufacturer · KR , Suwon

Weero Co., Ltd.

4 submissions · 4 cleared · Since 2024
4
Total
4
Cleared
0
Denied

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.

4 devices
1–4 of 4
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