Diamodent AA510
by Diamodent
Diamodent AA510 is a Class II device made by Diamodent, listed in FDA GUDID since 21 Dec 2018 (UDI-DI D907AA5100), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberD907AA5100 | Date21 Dec 2018 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Diamodent
- Generic name
- Dental implant suprastructure, permanent, preformed
- Description
- Compatible with: 3.5mm Narrow Platform (NP) NobelReplace implants Cement-On Post, Titanium 2mm Collar, 4.5mm Profile, Titefit
- Catalogue number
- AA510
- Primary DI / UDI-DI
- D907AA5100
- 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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