# K103577: Trinon Q & Q3 Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Trinon Titanium GmbH
- Decided: Jul 3, 2012 after 575 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 K052997 (2006). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062281: Zimmer One-Piece Implant, 4.7MM, Straight, Models ZOP47S10, ZOP47S11, ZOP47S13, ZOP47S16, Zimmer Dental, Inc. (2006) Summary page 1.
- K061717: Zimmer One-Piece Implant, 3.7 MM, Angled, Zimmer Dental, Inc. (2006) Summary page 1.
- K052997: Zimmer Dental One-Piece Implant, Zimmer Dental, Inc. (2006) Summary page 1.

## Indications for use
Trinon Q & Q3 Implant System is indicated for the support and retention of fixed single tooth and fixed partial denture restorations in the premolar, cuspid, and incisor regions of partially edentulous jaws. Trinon Q & Q3 Implant System might be loaded in the anterior mandibular arch if four are splinted together with a bar.

Source page: https://510kreport.com/device/K103577
Methodology: https://510kreport.com/methodology