Aesthetic Technology, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K240222 | Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) | June 4, 2024 |
| K212275 | Dermalux Flex MD | November 18, 2021 |
| K202028 | dermalux Flex MD | December 16, 2020 |
| K200659 | Dermalux Tri-Wave MD | May 9, 2020 |