Rhein Laser Technologies Co., Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Rhein Laser Technologies Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Wuhan, CN.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Rhein Laser Technologies Co., Ltd. Filter by specialty or product code using the sidebar.
3 devices
Cleared
Nov 19, 2024
Medical Thulium Fiber Laser Systems (UroFiber 60Q)
General & Plastic Surgery
109d
Cleared
Apr 11, 2024
TitanPico Laser Workstation (PICO-450)
General & Plastic Surgery
139d
Cleared
Feb 02, 2024
Artemis Diode Laser System (RL-S20S-TWC, RL-S20S-810B, RL-S20S-755)
General & Plastic Surgery
70d