Klockner 10 14 08
by Soadco, S.L.
Klockner 10 14 08 is a Class II device made by Soadco, S.L., cleared under FDA 510(k) K122988 on 19 Jul 2013 and listed in FDA GUDID since 30 Nov 2022 (UDI-DI 08435451602589), 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 | Number08435451602589 | Date30 Nov 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK122988 | Date19 Jul 2013 | StatusActive |
Official records
- AccessGUDID record 08435451602589
- FDA 510(k) database K122988
Across registries
- FDA 510(k) K122988 decided 19 Jul 2013 Active
- FDA GUDID UDI-DI 08435451602589 listed 30 Nov 2022 Listed
Timeline
- Cleared FDA 510(k) K122988
- Listed FDA GUDID 08435451602589
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Klockner
- Generic name
- Overdenture
- Model / Ref / Catalog
- 10 14 08
- Primary DI / UDI-DI
- 08435451602589
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Overdenture
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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