Shenzhen Goodwind Technology Development Co., Ltd. - FDA 510(k) Clear...
2
Total
2
Cleared
0
Denied
Shenzhen Goodwind Technology Development Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Dec 2025. 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.
2 devices