# K091907: Nobelprocera Implant Bridge Zirconia

- Pathway: 510(k) (Traditional)
- Applicant: Nobel Biocare AB
- Decided: Oct 6, 2009 after 103 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: 8 generations back to K944964 (1995). 62 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 68 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090069: Procera Implant Bridge Overdenture, Nobel Biocare AB (2009) Summary page 1.
- K053091: Procera Implant Bridge Zirconia, Nobel Biocare AB (2006) Summary page 1.

## Most influential descendants
- K160158: NobelProcera HT ML FCZ Implant Bridge and Framework (2016), 3 descendants of its own
- K202452: NobelProcera Zirconia Implant Bridge (2020), 2 descendants of its own
- K253999: Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic Screw (2026), 0 descendants of its own
- K240346: NobelProcera Zirconia Implant Bridge (2025), 0 descendants of its own
- K100356: TDS Precision Dental Bar (2010), 0 descendants of its own

## Indications for use
The NobelProcera Implant Bridge Zirconia is indicated for use as a bridge framework in the treatment of partially or totally edentulous jaws for the purpose of restoring chewing function.

Source page: https://510kreport.com/device/K091907
Methodology: https://510kreport.com/methodology