Solutis Slt
Solutis Slt is a Class II device made by Quantel Medical, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 03700542625453), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03700542625453 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 03700542625453
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Solutis
- Generic name
- Ophthalmic solid-state laser system, photodisruption
- Model / reference
- SLT
- Primary DI / UDI-DI
- 03700542625453
- FDA product code
- HQF
- GMDN term
- Ophthalmic solid-state laser system, photodisruption
- Device class
- Class II
- Regulation number
- 886.4390
- GUDID distribution status
- In Commercial Distribution
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