Lightlas SeLecTor Deux SLT0001
Lightlas SeLecTor Deux SLT0001 is a Class II device made by Lightmed Corporation, cleared under FDA 510(k) K090774 on 13 Aug 2009 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04712826770581), active as of 12 Nov 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 | Number04712826770581 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k) | NumberK090774 | Date13 Aug 2009 | StatusActive |
Official records
- AccessGUDID record 04712826770581
- FDA 510(k) database K090774
Across registries
- FDA 510(k) K090774 decided 13 Aug 2009 Active
- FDA GUDID UDI-DI 04712826770581 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K090774
- Listed FDA GUDID 04712826770581
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lightlas SeLecTor Deux
- Generic name
- General/multiple surgical frequency-doubled solid-state laser system
- Model / reference
- SLT0001
- Primary DI / UDI-DI
- 04712826770581
- 510(k) Number
- FDA product code
- HQF
- GMDN term
- General/multiple surgical frequency-doubled solid-state laser system
- Device class
- Class II
- Regulation number
- 886.4390
- GUDID distribution status
- In Commercial Distribution
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