# K925779: Branemark System Titanium Healing Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Nobelpharma USA, Inc.
- Decided: Apr 20, 1993 after 155 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
No predicates in its family tree.
551 later devices descend from it; 5 cite it directly.
0 of 552 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
- K962403: Noblepharma Wide Accessories (1996), 549 descendants of its own
- K971706: Tiadapt Abutment System (1997), 545 descendants of its own
- K974150: Procera Preparable Abutment System (1998), 543 descendants of its own
- K032263: 3I Patient-Specific Dental Abutment and Overdenture Bar (2004), 476 descendants of its own
- K042658: Procera Abutment Branemark, Models 10-4001, 10-4004, 10-5001, 10-5004, 10-6001, 10-6004 (2004), 441 descendants of its own

Source page: https://510kreport.com/device/K925779
Methodology: https://510kreport.com/methodology