Wondfo USA Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wondfo USA Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: WELLlife Flu A&B Home Test, WELLlife™ COVID-19 / Influenza A&B Home Test
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.
FDA 510(k) Regulatory Record - Wondfo USA Co., Ltd.
2 devices