# K151194: Klockner Dental Implant Abutments (II)

- Pathway: 510(k) (Abbreviated)
- Applicant: Soadco, S.L.
- Decided: Jan 29, 2016 after 270 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: 9 generations back to K894595 (1990). 122 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 127 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122988: Klockner Dental Implant Abutments, Soadco, S.L. (2013) Summary page 4.

## Most influential descendants
- K160850: Nucleoss Tpure Implant System (2017), 2 descendants of its own
- K231100: Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw (2024), 0 descendants of its own
- K230103: Klockner Abutments (2023), 0 descendants of its own
- K192062: Nucleoss T6 Dental Implant System (2020), 0 descendants of its own

## Indications for use
The Klockner Dental Implant Abutments are intended to be placed into dental implants to provide support for prosthetic reconstructions such as crowns, bridges. The Klockner Dental Implant Abutments include protective cap, temporary abutment, angled abutments, straight abutments, cast abutments. All abutments are intended to be used with the Klockner Dental Implant Systems, models: Essential EC, Essential EC 1.5.

Source page: https://510kreport.com/device/K151194
Methodology: https://510kreport.com/methodology