Shenzhen Lifotronic Technology Co., Ltd. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Lifotronic Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: H100Plus Hemoglobin Testing System, Diode Laser Hair Removal Machine (models: T60A, T60B, T60C, T60D, T60E), Air Compression Therapy System
3
Total
3
Cleared
0
Denied
Shenzhen Lifotronic Technology Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Oct 2026. Active since 2020.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Lifotronic Technology Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Qimmiq Medical Consulting Service Co., Ltd., Beijing Believe-Med Technology Service Co., Ltd. and Guangdong Grzan Group Co., Ltd..
FDA 510(k) Regulatory Record - Shenzhen Lifotronic Technology Co., Ltd.
3 devices