Neodent 140.961
by JJGC Indústria e Comércio de Materiais Dentários S/A.
Part of a family of 36 devices: see the family page
Ref 140.961Model IMPLANT
Neodent 140.961 is a device classified as Class IIb in the EU and Class II in the US made by JJGC Indústria e Comércio de Materiais Dentários S/A., registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI 987800075VW) and listed in FDA GUDID since 18 Aug 2017 (UDI-DI 07899878025061), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number987800075VW 07899878025061 | Date29 Apr 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07899878025061 | Date18 Aug 2017 | StatusListed |
Official records
- EUDAMED public site 987800075VW
- AccessGUDID record 07899878025061
Across registries
- EUDAMED Basic UDI-DI 987800075VW registered 29 Apr 2026 Active
- FDA GUDID UDI-DI 07899878025061 listed 18 Aug 2017 Listed
Timeline
- Listed FDA GUDID 07899878025061
- Registered EUDAMED 987800075VW
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Neodent
- Generic name
- Screw endosteal dental implant, one-piece
- Device name
- Drive Implants
- Model / Ref / Catalog
- 140.961, IMPLANT
- Primary DI / UDI-DI
- 07899878025061
- Basic UDI-DI
- 987800075VW
- FDA product code
- DZE
- EMDN code
- P01020101 Dental implants
- GMDN term
- Screw endosteal dental implant, one-piece
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 872.3640
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 3.5 MillimeterLength — 13 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIb | Class II |
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