# K071439: Zimmer Patient-Specific Abutment, Internal Hex, Titanium

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer Dental, Inc.
- Decided: Sep 20, 2007 after 120 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
No predicates in its family tree.
31 later devices descend from it; 6 cite it directly.
0 of 32 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) Zimmer® Hex-Lock Abutment, 3.5mm (cat. No. HLA3/3): named in the summary without a submission number

## Most influential descendants
- K120873: Zimmer ZFX Abutment for Nobel Replace Implant System (2012), 16 descendants of its own
- K134045: Zimmer ZFX Titanium Abutment, Base Abutment and Abutment Blank for Nobelactive Implant System (2014), 14 descendants of its own
- K141544: Zimmer ZFX Titanium Abutment for Biomet 3I Certain Implant System (2014), 12 descendants of its own
- K143505: Zimmer Patient-Specific Abutment, Internal Hex, Titanium (2015), 8 descendants of its own
- K181037: DIO CAD/CAM Abutment (2018), 7 descendants of its own

## Indications for use
The Zimmer® Patient Specific Abutment, Internal Hex, Titanium is used as a terminal or intermediate abutment for a cemented prosthesis. The abutment can be used for a single or multiple-unit restoration.

Source page: https://510kreport.com/device/K071439
Methodology: https://510kreport.com/methodology