# Rhein Laser Technologies Co., Ltd.

- Location (FDA's records): Wuhan, CN
- FDA decisions: 4 (2024–2026): 4 510(k) clearances
- Product codes: GEX (4)
- 510(k) review time since 2016: median 90 days, against 90 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Asclepion Laser Technologies GmbH: 2 (https://510kreport.com/company/asclepion-laser-technologies)
- Syneron Candela Corporation: 1 (https://510kreport.com/company/syneron-candela)
- Candela Corp.: 1 (https://510kreport.com/company/candela)
- Quanta System Spa: 1 (https://510kreport.com/company/quanta-system)

## Recent decisions
- K261738: Medical Thulium Fiber Laser Systems (UroFiber 150Q) (Jul 21, 2026)
- K242293: Medical Thulium Fiber Laser Systems (UroFiber 60Q) (Nov 19, 2024)
- K233757: TitanPico Laser Workstation  (PICO-450) (Apr 11, 2024)
- K233756: Artemis Diode Laser System (RL-S20S-TWC, RL-S20S-810B, RL-S20S-755) (Feb 2, 2024)

Source page: https://510kreport.com/company/rhein-laser-technologies