# K122807: Dental Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Hager& Meisinger GmbH
- Decided: Jun 13, 2014 after 652 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.
9 later devices descend from it; 2 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K143539: Dental Implant OKTAGON Bone Level (2015), 8 descendants of its own
- K173819: MyPlant II Implant System (2018), 3 descendants of its own
- K183024: Implacil Implant System (2020), 2 descendants of its own
- K170287: Dental Implants OKTAGON Bone Level Tapered Design (2017), 1 descendant of its own
- K202832: Implacil Implant System (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K122807
Methodology: https://510kreport.com/methodology