SD Abutment PMA-5030H
by Surgident
SD Abutment PMA-5030H is a Class II device made by Surgident, cleared under FDA 510(k) K173570 on 17 May 2019 and listed in FDA GUDID since 27 Jun 2019 (UDI-DI 08800041007349), 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 | Number08800041007349 | Date27 Jun 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173570 | Date17 May 2019 | StatusActive |
Official records
- AccessGUDID record 08800041007349
- FDA 510(k) database K173570
Across registries
- FDA 510(k) K173570 decided 17 May 2019 Active
- FDA GUDID UDI-DI 08800041007349 listed 27 Jun 2019 Listed
Timeline
- Cleared FDA 510(k) K173570
- Listed FDA GUDID 08800041007349
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SD Abutment
- Generic name
- Dental implant suprastructure, permanent, preformed
- Model / Ref / Catalog
- PMA-5030H, MA-5030H
- Primary DI / UDI-DI
- 08800041007349
- 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
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Unsafe
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