Anker Innovations Limited is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Anker Innovations Limited - FDA 510(k) Cleared Devices
Recent clearances: eufy Wearable Breast Pump (T600P, T6000, T6001, T6002, T6003, T6004, T6005, T6006, T6007, T6008, T6009), eufy Wearable Breast Pump S1 (T8D02)
2
Total
2
Cleared
0
Denied
Anker Innovations Limited has 2 FDA 510(k) cleared medical devices. Based in Hongkong, CN.
Latest FDA clearance: May 2026. 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.
FDA 510(k) Regulatory Record - Anker Innovations Limited
2 devices