Titan Implants I10C-4.2, 10
Titan Implants I10C-4.2, 10 (I10C-4.2,10) is a Class II device made by A.B. Dental Devices Ltd, cleared under FDA 510(k) K250806 on 18 Jun 2026 and listed in FDA GUDID since 16 Aug 2026 (UDI-DI 07290111270925), 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 | Number07290111270925 | Date16 Aug 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK250806 | Date18 Jun 2026 | StatusActive |
Official records
- AccessGUDID record 07290111270925
- FDA 510(k) database K250806
Across registries
- FDA 510(k) K250806 decided 18 Jun 2026 Active
- FDA GUDID UDI-DI 07290111270925 listed 16 Aug 2026 Listed
Timeline
- Cleared FDA 510(k) K250806
- Listed FDA GUDID 07290111270925
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Titan Implants
- Generic name
- Screw endosteal dental implant, two-piece
- Model / Ref / Catalog
- I10C-4.2, 10
- Primary DI / UDI-DI
- 07290111270925
- 510(k) Number
- FDA product code
- DZE
- GMDN term
- Screw endosteal dental implant, two-piece
- Device class
- Class II
- Regulation number
- 872.3640
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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