Beijing Winkonlaser Technology Limited
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-08-13
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253790 | High Intensity Focused Electromagnetic Stimulation Device (FE60) | NGX | 2026-08-13 | View |
| 510(k) | K241860 | Diode Laser Hair Removal System | GEX | 2024-09-25 | View |
No matching devices.