# K212775: Adin Short Implants

- Pathway: 510(k) (Traditional)
- Applicant: Adin Dental Implants Systems, Ltd.
- Decided: Jul 8, 2022 after 310 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.
No later device cites it as a predicate yet.
0 of 2 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 4.

## Indications for use
Adin Dental Implants are intended for surgical placement in the maxillary and/or mandibular arch to support crowns, bridges, or overdentures in fully or partially edentulous patients in order to restore a patient's chewing function. Adin Dental Implants may be immediately loaded when good primary stability is achieved and with appropriate occlusal loading. Adin short implants are to be used only with straight abutments.

Source page: https://510kreport.com/device/K212775
Methodology: https://510kreport.com/methodology