# K131165: Anker Dental Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Alliance Global
- Decided: Nov 14, 2013 after 204 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
Longest line of descent: 10 generations back to K894595 (1990). 30 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 32 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041368: Dentium CO., LTD. Implantium, Dentium Co., Ltd. (2004) Summary page 1.
- K091208: GS Iii System, Osstem Implant Co., Ltd. (2010) Summary page 3.

## Most influential descendants
- K142557: Anker Dental Implant System - SB-III, ST and AT series (2015), 0 descendants of its own

## Indications for use
Anker Dental Implant System is intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, and to restore the patient's chewing function. It is intended for delayed loading.

Source page: https://510kreport.com/device/K131165
Methodology: https://510kreport.com/methodology