# K132746: Nobelprocera Angulated Screw Channel Abutment Conical Connection

- Pathway: 510(k) (Traditional)
- Applicant: Nobel Biocare USA, LLC
- Decided: Jan 30, 2014 after 149 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
17 later devices descend from it; 4 cite it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K161655: On1 Concept (2017), 10 descendants of its own
- K181869: On1 Universal Abutment (2018), 6 descendants of its own
- K202344: TiUltra Implants and Xeal Abutments (2020), 4 descendants of its own
- K160158: NobelProcera HT ML FCZ Implant Bridge and Framework (2016), 3 descendants of its own
- K233208: NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium (2024), 2 descendants of its own

## Recalls of this device
- Mar 29, 2021 · Class II · Z-1680-2021: Not manufactured to specification
- Mar 29, 2021 · Class II · Z-1678-2021: Not manufactured to specification
- Mar 29, 2021 · Class II · Z-1681-2021: Not manufactured to specification
- Mar 29, 2021 · Class II · Z-1677-2021: Not manufactured to specification
- Mar 29, 2021 · Class II · Z-1679-2021: Not manufactured to specification

Source page: https://510kreport.com/device/K132746
Methodology: https://510kreport.com/methodology