Medical Device Manufacturer · CN , Xiamen

Manteia Technologies Co., Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2023

Total

Cleared

Denied

Manteia Technologies Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Xiamen, CN.

Latest FDA clearance: Aug 2026. Active since 2023. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Manteia Technologies Co., Ltd. Filter by specialty or product code using the sidebar.

Manteia Technologies Co., Ltd. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Manteia Technologies Co., Ltd.

7 devices

1-7 of 7