Klockner 18 05 43
by Soadco, S.L.
Klockner 18 05 43 is a Class II device made by Soadco, S.L., cleared under FDA 510(k) K153098 on 8 Apr 2016 and listed in FDA GUDID since 14 Jul 2022 (UDI-DI 08435451604989), 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 | Number08435451604989 | Date14 Jul 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK153098 | Date8 Apr 2016 | StatusActive |
Official records
- AccessGUDID record 08435451604989
- FDA 510(k) database K153098
Across registries
- FDA 510(k) K153098 decided 8 Apr 2016 Active
- FDA GUDID UDI-DI 08435451604989 listed 14 Jul 2022 Listed
Timeline
- Cleared FDA 510(k) K153098
- Listed FDA GUDID 08435451604989
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Klockner
- Generic name
- Intramucosal dental implant
- Model / Ref / Catalog
- 18 05 43
- Primary DI / UDI-DI
- 08435451604989
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Intramucosal dental implant
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Intramucosal dental implant.