Klockner 10 14 01
by Soadco, S.L.
Klockner 10 14 01 is a Class II device made by Soadco, S.L., cleared under FDA 510(k) K080224 on 3 Jul 2008 and listed in FDA GUDID since 30 Nov 2022 (UDI-DI 08435451602510), 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 | Number08435451602510 | Date30 Nov 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK080224 | Date3 Jul 2008 | StatusActive |
Official records
- AccessGUDID record 08435451602510
- FDA 510(k) database K080224
Across registries
- FDA 510(k) K080224 decided 3 Jul 2008 Active
- FDA GUDID UDI-DI 08435451602510 listed 30 Nov 2022 Listed
Timeline
- Cleared FDA 510(k) K080224
- Listed FDA GUDID 08435451602510
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- Withdrawn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 01
- Primary DI / UDI-DI
- 08435451602510
- 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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