Orthovisc 277500
Orthovisc 277500 is a Class III device made by Saima Global Farma S.L., approved under FDA PMA P030019 on 4 Feb 2004 and listed in FDA GUDID since 13 Nov 2024 (UDI-DI 08437027710025), active as of 23 Oct 2026.
Active
PMA
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08437027710025 | Date13 Nov 2024 | StatusListed |
| United States | FDA PMAAPPR | NumberP030019 | Date4 Feb 2004 | StatusActive |
Official records
- AccessGUDID record 08437027710025
- FDA PMA database P030019
Across registries
- FDA PMA P030019 decided 4 Feb 2004 Active
- FDA GUDID UDI-DI 08437027710025 listed 13 Nov 2024 Listed
Timeline
- Approved FDA PMA P030019
- Listed FDA GUDID 08437027710025
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA PMA Active
Specification
- Trade name
- Orthovisc
- Generic name
- Synovial fluid supplementation medium
- Model / reference
- 277500
- Primary DI / UDI-DI
- 08437027710025
- PMA number
- FDA product code
- MOZ
- GMDN term
- Synovial fluid supplementation medium
- Device class
- Class III
- GUDID distribution status
- In Commercial Distribution
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