Optisource 74-0323-G
by Phoenix Healthcare Solutions, LLC
Optisource 74-0323-G is a Class II device made by Phoenix Healthcare Solutions, LLC, cleared under FDA 510(k) K231123 on 30 Aug 2023 and listed in FDA GUDID since 18 Aug 2024 (UDI-DI 00817096001435), 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 | Number00817096001435 | Date18 Aug 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK231123 | Date30 Aug 2023 | StatusActive |
Official records
- AccessGUDID record 00817096001435
- FDA 510(k) database K231123
Across registries
- FDA 510(k) K231123 decided 30 Aug 2023 Active
- FDA GUDID UDI-DI 00817096001435 listed 18 Aug 2024 Listed
Timeline
- Cleared FDA 510(k) K231123
- Listed FDA GUDID 00817096001435
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Optisource
- Generic name
- Contact lens case
- Model / reference
- 74-0323-G
- Primary DI / UDI-DI
- 00817096001435
- FDA product code
- LRX
- GMDN term
- Contact lens case
- Device class
- Class II
- Regulation number
- 886.5928
- GUDID distribution status
- In Commercial Distribution
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