# K252031: Adin Long Dental Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Adin Dental Implant Systems, Ltd.
- Decided: Mar 23, 2026 after 266 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: 17 generations back to K960026 (1996). 260 ancestors in all.
No later device cites it as a predicate yet.
0 of 261 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151909: Noris Medical Zygomatic Dental Implant System, Noris Medical, Ltd. (2016) Summary page 5.

## Indications for use
The Adin Long Dental Implant System is intended to be surgically placed in the bone of the upper jaw arches to provide support for prosthetic devices such as artificial teeth in order to restore the patient's chewing function in fully or partially edentulous patients. The implants are intended for multi-unit, full-arch, screw-retained prosthetic restorations and may be loaded immediately when good primary stability is achieved and with appropriate occlusal loading. Adin Touareg-OS Zygomatic Dental Implants are intended for placement in the zygomatic bone in patients with severe atrophic maxilla; they may be used with implant-level framework designs with 45° to 60° angulation.

Source page: https://510kreport.com/device/K252031
Methodology: https://510kreport.com/methodology