Wondfo USA Co., Ltd. - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Wondfo USA Co, Ltd. as regulatory consultant.
2 devices