Shenzhen Leaflife Technology Co., Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Shenzhen Leaflife Technology Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Nov 2025. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Leaflife Technology Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Shenzhen Leaflife Technology Co., Ltd.
7 devices
Cleared
Nov 25, 2025
LeafPure-Echo (LM-LPNdA)
General & Plastic Surgery
57d
Cleared
Aug 14, 2025
WinForth (LM-E470KA)
General & Plastic Surgery
140d
Cleared
Feb 20, 2024
Mjolnir Pro. (Multi–electrode plasma)
General & Plastic Surgery
88d
Cleared
Sep 11, 2023
Planar LED mate
General & Plastic Surgery
213d
Cleared
Apr 12, 2022
LED Therapy Device (Planar LED/Planar LED mini)
General & Plastic Surgery
90d
Cleared
Nov 19, 2021
Leaf Smooth
General & Plastic Surgery
86d
Cleared
Nov 19, 2020
Laser Therapy Device
General & Plastic Surgery
50d