# K230103: Klockner Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Soadco, S.L.
- Decided: Apr 24, 2023 after 101 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K894595 (1990). 123 ancestors in all.
No later device cites it as a predicate yet.
0 of 124 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151194: Klockner Dental Implant Abutments (II), Soadco, S.L. (2016) Summary page 4.

## Indications for use
Klockner Abutments are intended for use in dental implants to provide a support structure so that the edentulous or partially edentulous patients will regain their masticatory and aesthetic functions. All digitally designed abutments for use with Klockner TiBase Abutments are intended to be sent to a SOADCO S.L. validated milling center for manufacture.

Source page: https://510kreport.com/device/K230103
Methodology: https://510kreport.com/methodology