Voyager DSLT 430840610
Voyager DSLT 430840610 is an ophthalmic solid-state laser system (FDA Class II; FDA product code HQF, Laser, Ophthalmic) made by Belkin Vision, Ltd., cleared under FDA 510(k) K230722 on 8 Dec 2023 and listed in FDA GUDID since 16 Jul 2025 (UDI-DI 07290018686058), active as of 23 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 | Number07290018686058 | Date16 Jul 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK230722 | Date8 Dec 2023 | StatusActive |
Official records
- AccessGUDID record 07290018686058
- FDA 510(k) database K230722
Across registries
- FDA 510(k) K230722 decided 8 Dec 2023 Active
- FDA GUDID UDI-DI 07290018686058 listed 16 Jul 2025 Listed
Timeline
- Cleared FDA 510(k) K230722
- Listed FDA GUDID 07290018686058
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Voyager DSLT
- Generic name
- Ophthalmic solid-state laser system
- Model / reference
- 430840610
- Primary DI / UDI-DI
- 07290018686058
- 510(k) Number
- FDA product code
- HQF
- GMDN term
- Ophthalmic solid-state laser system
- Device class
- Class II
- Regulation number
- 886.4390
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Ophthalmic solid-state laser system.