ATL eBeam
by Advanced Technology Laser Co., Ltd.
ATL eBeam is a Class II device made by Advanced Technology Laser Co., Ltd., cleared under FDA 510(k) K101555 on 17 Sep 2010 and listed in FDA GUDID since 26 Oct 2016 (UDI-DI 06970507240121), 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 | Number06970507240121 | Date26 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK101555 | Date17 Sep 2010 | StatusActive |
Official records
- AccessGUDID record 06970507240121
- FDA 510(k) database K101555
Across registries
- FDA 510(k) K101555 decided 17 Sep 2010 Active
- FDA GUDID UDI-DI 06970507240121 listed 26 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K101555
- Listed FDA GUDID 06970507240121
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Atl
- Generic name
- Dermatological carbon dioxide laser system
- Model / reference
- eBeam
- Primary DI / UDI-DI
- 06970507240121
- 510(k) Number
- FDA product code
- GEX
- GMDN term
- Dermatological carbon dioxide laser system
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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