Anker Innovations Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Anker Innovations Limited has 1 FDA 510(k) cleared medical devices. Based in Hongkong, CN.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Anker Innovations Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Joyantech Consulting Co., Ltd. as regulatory consultant.
1 devices