# K062876: Primaconnex Ceramic Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Lifecore Biomedical, Inc.
- Decided: Nov 1, 2006 after 36 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 K960026 (1996). 44 ancestors in all.
6 later devices descend from it; 2 cite it directly.
0 of 51 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051614: Primaconnex Internal Connection Implant System, Primaconnex Internal Connection Prosthetics, Lifecore Biomedical, Inc. (2005) Summary page 2.
- K060530: SD Ceramic Coping for Quick Abutment, Locking. Model 45301.  RD Ceramic Coping for Quick Abutment, Locking, Model 45302., Lifecore Biomedical, Inc. (2006) Summary page 1.
- K023631: Astra Tech Dental Implants-Ceramic Abutments, Astra Tech, Inc. (2002) Summary page 1.

## Most influential descendants
- K103020: Atlantis Abutment for Keystone Implant, Atlantis Gemini Abutment (2011), 4 descendants of its own
- K161713: Dentium CAD/CAM Abutments (2016), 3 descendants of its own
- K251605: DIMPLO Implant System (2025), 0 descendants of its own
- K221972: Warantec Custom Abutment (2023), 0 descendants of its own
- K171622: Dentium Ti-Base (2018), 0 descendants of its own

## Indications for use
PrimaConnex Ceramic Abutments are intended for use in conjunction with the PrimaConnex Internal Connection Inplant System in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit cement retained restorations.

Source page: https://510kreport.com/device/K062876
Methodology: https://510kreport.com/methodology