Shanghai Omni Laser Skinology 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 |
|---|
| K230342 | Phototherapy System (OL-PDT950) | August 16, 2023 |
| K223778 | Diode Laser Hair Removal System (RD-SLD600) | March 31, 2023 |
| K220214 | Painless IPL System - KDT750 | February 18, 2023 |