Rexall DG11
Rexall DG11 is a Class II device made by Watchdog Group, LC, cleared under FDA 510(k) K130753 on 13 Jun 2013 and listed in FDA GUDID since 6 Oct 2016 (UDI-DI 00897522001505), 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 | Number00897522001505 | Date6 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK130753 | Date13 Jun 2013 | StatusActive |
Official records
- AccessGUDID record 00897522001505
- FDA 510(k) database K130753
Across registries
- FDA 510(k) K130753 decided 13 Jun 2013 Active
- FDA GUDID UDI-DI 00897522001505 listed 6 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K130753
- Listed FDA GUDID 00897522001505
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Rexall
- Generic name
- Contact lens case
- Model / reference
- DG11
- Primary DI / UDI-DI
- 00897522001505
- 510(k) Number
- 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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