Shenzhen Goodwind Technology Development Co., Ltd. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Goodwind Technology Development Co., Ltd. - FDA 510(k) Clear...
Recent clearances: Eye Recovery Pro (PH-e03), Wrinkle Retreat Pro Light Therapy Face Mask (Model: PH-m03), IPL Hair Removal Device
3
Total
3
Cleared
0
Denied
Shenzhen Goodwind Technology Development Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Aug 2026. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Goodwind Technology Development Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Feiying Drug & Medical Consulting Technical Service Group as regulatory consultant.
FDA 510(k) Regulatory Record - Shenzhen Goodwind Technology Development Co., Ltd.
3 devices