Medical Device Manufacturer · US , San Diego , CA

Wondfo USA Co., Ltd.

2 submissions · 2 cleared · Since 2025
2
Total
2
Cleared
0
Denied

Wondfo USA Co., Ltd. — FDA 510(k) Submissions

Wondfo USA Co., Ltd. has submitted 2 FDA 510(k) premarket notifications since 2025, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Multi-analyte Respiratory Virus Antigen Detection Test . Use the specialty filter in the sidebar to narrow results.

2 devices
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