ATL SoomthTouch
by Advanced Technology Laser Co., Ltd.
ATL SoomthTouch is a Class II device made by Advanced Technology Laser Co., Ltd., cleared under FDA 510(k) K140249 on 8 Oct 2014 and listed in FDA GUDID since 20 Oct 2016 (UDI-DI 06970507240213), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06970507240213 | Date20 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK140249 | Date8 Oct 2014 | StatusActive |
Official records
- AccessGUDID record 06970507240213
- FDA 510(k) database K140249
Across registries
- FDA 510(k) K140249 decided 8 Oct 2014 Active
- FDA GUDID UDI-DI 06970507240213 listed 20 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K140249
- Listed FDA GUDID 06970507240213
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Atl
- Generic name
- Dermatological solid-state laser system
- Model / reference
- SoomthTouch
- Primary DI / UDI-DI
- 06970507240213
- 510(k) Number
- FDA product code
- GEX
- GMDN term
- Dermatological solid-state laser system
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices in this category
Other devices filed under Dermatological solid-state laser system.