Klockner 18 16 24
by Soadco, S.L.
Klockner 18 16 24 is a Class II device made by Soadco, S.L., cleared under FDA 510(k) K230103 on 24 Apr 2023 and listed in FDA GUDID since 13 Jun 2023 (UDI-DI 08435451634962), 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 | Number08435451634962 | Date13 Jun 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK230103 | Date24 Apr 2023 | StatusActive |
Official records
- AccessGUDID record 08435451634962
- FDA 510(k) database K230103
Across registries
- FDA 510(k) K230103 decided 24 Apr 2023 Active
- FDA GUDID UDI-DI 08435451634962 listed 13 Jun 2023 Listed
Timeline
- Cleared FDA 510(k) K230103
- Listed FDA GUDID 08435451634962
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Klockner
- Generic name
- Overdenture
- Model / Ref / Catalog
- 18 16 24
- Primary DI / UDI-DI
- 08435451634962
- 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
Similar devices
Other devices filed under FDA product code NHA (Abutment, implant, dental, endosseous).
- s-Clean Link Abutment DSLARC451047HS by DENTIS CO., LTD
- Atlantis Abutment in Zirconia for Astra Tech Osseospeed Plus Implant by Astra Tech, Inc.
- Biotem SAAT65747 by Biotem Co., ltd
- Equator Abutment, Φ 4.8mm, GH 1mm 034010 by BIO CONCEPT Co., Ltd.
- s-Clean Link Abutment DSLAR485045HS by DENTIS CO., LTD
- Biotem HAA455M by Biotem Co., ltd
- TruAbutment DS, TruBase S by TruAbutment Inc.
- Neobiotech Implant System ISAE517 by Neobiotech Co.,Ltd.
- Angular Abutment NM-A2404 by NORIS MEDICAL LTD
- Warantec Custom Abutment by WARANTEC.Co., Ltd