Rhein Laser Technologies Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Rhein Laser Technologies Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Medical Thulium Fiber Laser Systems (UroFiber 60Q), TitanPico Laser Workstation (PICO-450), Artemis Diode Laser System (RL-S20S-TWC, RL-S20S-810B, RL-S20S-755)
4
Total
4
Cleared
0
Denied
Rhein Laser Technologies Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Wuhan, CN.
Latest FDA clearance: Jul 2026. 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.
FDA 510(k) Regulatory Record - Rhein Laser Technologies Co., Ltd.
4 devices
Cleared
Jul 21, 2026
Medical Thulium Fiber Laser Systems (UroFiber 150Q)
General & Plastic Surgery
55d
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