Temporary Abutment ICTAHR4092ES
Temporary Abutment ICTAHR4092ES is a Class II device made by Cybermed Inc., cleared under FDA 510(k) K210039 on 7 Jan 2022 and listed in FDA GUDID since 31 Oct 2022 (UDI-DI 08800023144215), active as of 23 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 | Number08800023144215 | Date31 Oct 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK210039 | Date7 Jan 2022 | StatusActive |
Official records
- AccessGUDID record 08800023144215
- FDA 510(k) database K210039
Across registries
- FDA 510(k) K210039 decided 7 Jan 2022 Active
- FDA GUDID UDI-DI 08800023144215 listed 31 Oct 2022 Listed
Timeline
- Cleared FDA 510(k) K210039
- Listed FDA GUDID 08800023144215
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Temporary Abutment
- Generic name
- Dental implant suprastructure, permanent, preformed
- Model / reference
- ICTAHR4092ES
- Primary DI / UDI-DI
- 08800023144215
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Dental implant suprastructure, permanent, preformed
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution