Diamodent P510
by Diamodent
Diamodent P510 is a Class II device made by Diamodent, cleared under FDA 510(k) K010619 on 28 Sep 2001 and listed in FDA GUDID since 19 Dec 2018 (UDI-DI D907P5100), 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 | NumberD907P5100 | Date19 Dec 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK010619 | Date28 Sep 2001 | StatusActive |
Official records
- FDA 510(k) database K010619
Across registries
- FDA 510(k) K010619 decided 28 Sep 2001 Active
- FDA GUDID UDI-DI D907P5100 listed 19 Dec 2018 Listed
Timeline
- Cleared FDA 510(k) K010619
- Listed FDA GUDID D907P5100
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Diamodent
- Generic name
- Dental implant suprastructure, permanent, preformed
- Description
- Compatible with: 3.5mm Platform Screw-Vent Zimmer implants Cement-On Post, Titanium 2mm Collar, 4.5mm Profile, TiteFit
- Catalogue number
- P510
- Primary DI / UDI-DI
- D907P5100
- 510(k) Number
- FDA product code
- DZE
- GMDN term
- Dental implant suprastructure, permanent, preformed
- Device class
- Class II
- Regulation number
- 872.3640
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Dry Heat Sterilization
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