# K010132: Klockner Dental Implants, Models SK, NK, IK, S3, and S4

- Pathway: 510(k) (Traditional)
- Applicant: Soadco, S.L.
- Decided: Jun 4, 2002 after 504 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 2 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K080224: Klockner Essential Dental Implants System, Models Essential Cone (EC), Essential Solid (ES) and Eck (2008), 11 descendants of its own
- K082200: Klockner Essential Dental Implants System, Model Essential Cone 1.5 (2008), 10 descendants of its own
- K122988: Klockner Dental Implant Abutments (2013), 9 descendants of its own
- K151194: Klockner Dental Implant Abutments (II) (2016), 4 descendants of its own
- K160221: Implance Dental Implant System, Implance Dental Abutment System (2016), 3 descendants of its own

Source page: https://510kreport.com/device/K010132
Methodology: https://510kreport.com/methodology