Lotuxs Medtech (Suzhou) Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K222862 | SILKPRO Titanium Diode Laser System SILKPRO-S20S-TWC | July 30, 2023 |
| K211402 | Powersculp laser lipolysis system | July 30, 2021 |