Sanhe Lefis Electronics 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 |
|---|
| K261204 | Intense Pulsed Light Therapy Device | June 12, 2026 |
| K250998 | CO2 Laser Therapy System (Model: LFS-D9U) | December 19, 2025 |
| K252319 | Q-Switched Nd: YAG Laser machine (LFS-C13U) | October 20, 2025 |