Supartz
Supartz is a Class III device made by Ally Medical Supplies Ltd, approved under FDA PMA P980044 on 24 Jan 2001 and listed in FDA GUDID since 13 Sep 2016 (UDI-DI 05060459970120), active as of 22 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 | Number05060459970120 | Date13 Sep 2016 | StatusListed |
| United States | FDA PMAAPPR | NumberP980044 | Date24 Jan 2001 | StatusActive |
Official records
- AccessGUDID record 05060459970120
- FDA PMA database P980044
Across registries
- FDA PMA P980044 decided 24 Jan 2001 Active
- FDA GUDID UDI-DI 05060459970120 listed 13 Sep 2016 Listed
Timeline
- Approved FDA PMA P980044
- Listed FDA GUDID 05060459970120
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA PMA Active
Specification
- Generic name
- Synovial fluid supplementation medium
- Primary DI / UDI-DI
- 05060459970120
- 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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