Rhein Laser Technologies Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242293 | Medical Thulium Fiber Laser Systems (UroFiber 60Q) | November 19, 2024 |
| K233757 | TitanPico Laser Workstation (PICO-450) | April 11, 2024 |
| K233756 | Artemis Diode Laser System (RL-S20S-TWC, RL-S20S-810B, RL-S20S-755) | February 2, 2024 |