Medical Device Manufacturer · US , San Diego , CA

Wondfo USA Co., Ltd. - FDA 510(k) Cleared Devices

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

Wondfo USA Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.

Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Wondfo USA Co., Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Wondfo USA Co., Ltd.

2 devices
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All2 Microbiology 2