Diamodent AB1010
by Diamodent
Diamodent AB1010 is a Class II device made by Diamodent, listed in FDA GUDID since 4 Jan 2019 (UDI-DI D907AB10100), 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 | NumberD907AB10100 | Date4 Jan 2019 | 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- Withdrawn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: 4.3mm Regular Platform (RP) NobelReplace implants Zirconia Abutment Base, Titanium, Yellow Engaging, 0.35 Collar, 4.8mm Profile, 5.0mm Height
- Catalogue number
- AB1010
- Primary DI / UDI-DI
- D907AB10100
- 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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