# K112585: Touareg Closefit Dental Impant System

- Pathway: 510(k) (Special)
- Applicant: Adin Dental Implants System, Ltd.
- Decided: May 24, 2012 after 261 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: 1 generation back to K081751 (2008). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081751: Adin Dental Implants System, Adin Dental Implants System, Ltd. (2008) Summary page 1.

## Most influential descendants
- K223714: UniFit Dental Implant System (2023), 1 descendant of its own
- K250178: Adin Customized Abutments (2025), 0 descendants of its own

## Indications for use
Touareg CloseFitTM Dental Implants are intended for surgical placement in the maxillary and/or mandibular arch to support crowns, bridges, or overdentures in edentulous or partially edentulous patients. Touareg CloseFitTM Dental Implants may be immediately loaded when good primary stability is achieved and with appropriate occlusal loading

Source page: https://510kreport.com/device/K112585
Methodology: https://510kreport.com/methodology