# K120954: Nobelprocera Peek Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Nobel Biocare AB
- Decided: Jun 5, 2013 after 432 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: 3 generations back to K891615 (1989). 8 ancestors in all.
105 later devices descend from it; 4 cite it directly.
0 of 114 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K925766: Branemark System Temporary Solutions, Nobelpharma USA, Inc. (1994) Summary page 1.
- K043195: Neo Implant System, Neoss, Ltd. (2005) Summary page 1.

## Most influential descendants
- K133731: Nobelactive Wide Platform (WP) (2014), 101 descendants of its own
- K142260: NobelActive (2015), 99 descendants of its own
- K170588: DESS Dental Smart Solutions (2017), 86 descendants of its own
- K173908: DESS Dental Smart Solutions (2018), 51 descendants of its own
- K191986: DESS Dental Smart Solutions (2019), 38 descendants of its own

## Indications for use
The Nobel Biocare PEEK Abutments are premanufactured prosthetic components directly connected to endosseous dental implants and are intended for provisional use up to 180 days as an aid in prosthetic rehabilitation.

Source page: https://510kreport.com/device/K120954
Methodology: https://510kreport.com/methodology