# K130694: JR Implant System

- Pathway: 510(k) (Traditional)
- Applicant: LK Consulting Group USA, Inc.
- Decided: Jun 19, 2014 after 462 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: 8 generations back to K894595 (1990). 22 ancestors in all.
No later device cites it as a predicate yet.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062566: Nobelreplace Tapered Conical Connection, Nobel Biocare USA, LLC (2006) Summary page 1.

## Indications for use
The JR Implant System is indicated for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations including; cemented retained, screw retained, or overdenture restorations, and terminal or intermediate abutment support for fixed bridgework. The JR Implant System is for single and two stage surgical procedures. These systems are intended for delayed loading.

Source page: https://510kreport.com/device/K130694
Methodology: https://510kreport.com/methodology