Klockner 84 01 07
by Soadco, S.L.
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08435451627490 | Date13 Jun 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK230103 | Date24 Apr 2023 | StatusActive |
Official records
- AccessGUDID record 08435451627490
- FDA 510(k) database K230103
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Klockner
- Generic name
- Dental implant suprastructure kit
- Model / Ref / Catalog
- 84 01 07
- Primary DI / UDI-DI
- 08435451627490
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Dental implant suprastructure kit
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Other devices from Soadco, S.L.
Properties
Other properties (11)
- Supplied sterile: No
- Implantable: No
- Contains latex: No
- Prescription use: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No
- Serial number: No
- Expiration date: No