Aesthetic Technology, Ltd.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories3
Latest FDA decision2024-06-04
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240222 | Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) | GEX | 2024-06-04 | View |
| 510(k) | K212275 | Dermalux Flex MD | OHS | 2021-11-18 | View |
| 510(k) | K202028 | dermalux Flex MD | ILY | 2020-12-16 | View |
| 510(k) | K200659 | Dermalux Tri-Wave MD | GEX | 2020-05-09 | View |
No matching devices.