Manteia Technologies Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Manteia Technologies Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: AccuContour 4.0, ARTAssistant, AccuCheck
6
Total
6
Cleared
0
Denied
Manteia Technologies Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Xiamen, CN.
Latest FDA clearance: Jan 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.
FDA 510(k) Regulatory Record - Manteia Technologies Co., Ltd.
6 devices