# K134045: Zimmer ZFX Titanium Abutment, Base Abutment and Abutment Blank for Nobelactive Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer Dental, Inc.
- Decided: Apr 25, 2014 after 115 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K894595 (1990). 77 ancestors in all.
14 later devices descend from it; 3 cite it directly.
0 of 92 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120873: Zimmer ZFX Abutment for Nobel Replace Implant System, Zimmer Dental, Inc. (2012) Summary page 1.
- K091756: Nobelprocera TI Abutment, Nobel Biocare AB (2009) Summary page 1.
- K071370: Nobelactive Internal Connection Implant, Nobel Biocare AB (2007) Summary page 1.

## Most influential descendants
- 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
- K160850: Nucleoss Tpure Implant System (2017), 2 descendants of its own
- K222913: s-Clean Link Abutment (2023), 1 descendant of its own

## Indications for use
The Zimmer Zfx Titanium Abutment for NobelActive Implant System is designed for use as a terminal or intermediate abutment for cement retained prostheses. The abutment can be used with NobelActive and NobeiReplace Conical Connection implants with a Narrow Platform (NP) 0 3.5mm or Regular Platform (RP) 0 3.9mm

Source page: https://510kreport.com/device/K134045
Methodology: https://510kreport.com/methodology