Guangzhou Aimooe Technology Co., Ltd. is one of 2194 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Guangzhou Aimooe Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Disposable Reflective Marker Spheres (AM-BK115S, AM-BL130S)
1
Total
1
Cleared
0
Denied
Guangzhou Aimooe Technology Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Guangzhou, CN.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Guangzhou Aimooe Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Share Info (Guangzhou) Medical Consultant , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Guangzhou Aimooe Technology Co., Ltd.
1 devices