Wuhan Pioon Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K243764 | Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W) | May 8, 2025 |
| K250656 | Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75) | April 4, 2025 |
| K240747 | Medical Diode Laser (M2-GK) | June 17, 2024 |
| K240644 | Medical Diode Laser (S1Pro) | June 10, 2024 |
| K240179 | Medical Diode Laser (Model: L2) | March 21, 2024 |
| K231548 | Medical Diode Laser, Model S1Pro | August 3, 2023 |
| K230274 | Medical Diode Laser (M2) | March 31, 2023 |