Weifang Mingliang 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 |
| K260307 | Diode Laser Therapy Systems (V19) | April 15, 2026 |
| K242183 | Fractional CO2 Laser Therapy System (EXFU CO2) | October 23, 2024 |
| K200525 | Medical Diode Laser Hair Removal System | May 27, 2020 |