Acuity DN550-Uv-23.5
Active
PMA
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM454DN550UVP2351 | Date18 Sep 2015 | StatusListed |
| United States | FDA PMAAPPR | NumberP880072 | Date22 Sep 1989 | StatusActive |
Recalls
No FDA recalls found in the data synced 8 Nov 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA PMA Active
Specification
- Trade name
- Acuity
- Generic name
- Posterior-chamber intraocular lens, pseudophakic
- Model / reference
- DN550-UV-23.5
- Primary DI / UDI-DI
- M454DN550UVP2351
- PMA number
- FDA product code
- HQL
- GMDN term
- Posterior-chamber intraocular lens, pseudophakic
- Device class
- Class III
- Regulation number
- 886.3600
- GUDID distribution status
- In Commercial Distribution
Other devices from Eyekon Medical Inc.
Properties
Other properties (7)
- Sterilise before use: No
- Contains latex: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No