SD Abutment N-HA4015
by Surgident
SD Abutment N-HA4015 is a Class II device made by Surgident, cleared under FDA 510(k) K173570 on 17 May 2019 and listed in FDA GUDID since 24 Feb 2020 (UDI-DI 08800041008223), 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 | Number08800041008223 | Date24 Feb 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173570 | Date17 May 2019 | StatusActive |
Official records
- AccessGUDID record 08800041008223
- FDA 510(k) database K173570
Across registries
- FDA 510(k) K173570 decided 17 May 2019 Active
- FDA GUDID UDI-DI 08800041008223 listed 24 Feb 2020 Listed
Timeline
- Cleared FDA 510(k) K173570
- Listed FDA GUDID 08800041008223
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SD Abutment
- Generic name
- Dental implant suprastructure, temporary, preformed, single-use
- Model / Ref / Catalog
- N-HA4015
- Primary DI / UDI-DI
- 08800041008223
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Dental implant suprastructure, temporary, preformed, single-use
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Unsafe
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