Anatomic Abutment Sap-1503
by Dentin Implants Technologies Ltd
Anatomic Abutment Sap-1503 is a Class II device made by Dentin Implants Technologies Ltd, cleared under FDA 510(k) K120530 on 5 Jul 2012 and listed in FDA GUDID since 30 Jul 2019 (UDI-DI 07290113356870), 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 | Number07290113356870 | Date30 Jul 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK120530 | Date5 Jul 2012 | StatusActive |
Official records
- AccessGUDID record 07290113356870
- FDA 510(k) database K120530
Across registries
- FDA 510(k) K120530 decided 5 Jul 2012 Active
- FDA GUDID UDI-DI 07290113356870 listed 30 Jul 2019 Listed
Timeline
- Cleared FDA 510(k) K120530
- Listed FDA GUDID 07290113356870
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Anatomic Abutment
- Generic name
- Dental implant suprastructure, permanent, preformed
- Model / reference
- SAP-1503
- Primary DI / UDI-DI
- 07290113356870
- 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
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