Lifemotion Medical Technology Co., Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lifemotion Medical Technology Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lifemotion Medical Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MEDIcept, Inc. as regulatory consultant.
1 devices