# K062519: NEXUS 3

- Pathway: 510(k) (Traditional)
- Applicant: Kerr Corporation
- Decided: Oct 19, 2006 after 52 days
- Product code: EMA (Cement, Dental)
- Device class: 2
- Regulation: 21 CFR 872.3275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Nexus 2: named in the summary without a submission number

## Most influential descendants
- K110508: Suglue-10 (2011), 8 descendants of its own
- K153231: G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi Primer (2016), 5 descendants of its own
- K200798: G-Cem One (2020), 3 descendants of its own
- K254109: G-Cem Universal (2026), 0 descendants of its own
- K254063: iCEM Universal Plus (2025), 0 descendants of its own

## Indications for use
Nexus 3 is a resin cement for the cementation of ceramic, resin, and metal-based veneers, inlays, onlays, crowns, bridges and posts, bonding of amalgam restorations, and as core-buildup material.

Source page: https://510kreport.com/device/K062519
Methodology: https://510kreport.com/methodology