Lotuxs Medtech (Suzhou) Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-07-30
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222862 | SILKPRO Titanium Diode Laser System SILKPRO-S20S-TWC | GEX | 2023-07-30 | View |
| 510(k) | K211402 | Powersculp laser lipolysis system | PKT | 2021-07-30 | View |
No matching devices.