# K233208: NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium

- Pathway: 510(k) (Traditional)
- Applicant: Nobel Biocare AB
- Decided: Jan 24, 2024 after 118 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: 9 generations back to K894595 (1990). 75 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 78 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091756: Nobelprocera TI Abutment, Nobel Biocare AB (2009) Summary page 6.
- K132746: Nobelprocera Angulated Screw Channel Abutment Conical Connection, Nobel Biocare USA, LLC (2014) Summary page 6.

## Most influential descendants
- 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
- K231566: ICX-Implant System (2024), 0 descendants of its own

## Indications for use
NobelProcera® Abutment Titanium is a patient-matched CAD/CAM prosthetic component directly connected to endosseous dental implants and is indicated for use as an aid in prosthetic rehabilitation. Clinical and Abutment Screws are indicated for use to secure a dental abutment or framework to a dental implant in the maxilla or mandible for supporting tooth replacements and are indicated as an aid in prosthetic rehabilitation.

Source page: https://510kreport.com/device/K233208
Methodology: https://510kreport.com/methodology