Beijing Superlaser Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251457 | Diode laser therapy device (VADER) | September 3, 2025 |
| K200042 | CO2 Laser System | June 9, 2020 |
| K193464 | ND:YAG Laser | April 13, 2020 |
| K192516 | Diode Laser 808nm | December 10, 2019 |
| K192519 | Multi-modality workstation | November 27, 2019 |