# K926501: Branemark System (R) - 5.5MM Fixture

- Pathway: 510(k) (Traditional)
- Applicant: Nobelpharma USA, Inc.
- Decided: Oct 5, 1993 after 280 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
30 later devices descend from it; 2 cite it directly.
0 of 31 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
- K955281: Endosseous Dental Implant & Accessories (1996), 27 descendants of its own
- K061169: Endosseous Dental Implant (2006), 24 descendants of its own
- K070841: Endosseous Dental Implant System (2007), 21 descendants of its own
- K070905: Endosseous Dental Implant System (2007), 17 descendants of its own
- K163634: External Hex Implants (2017), 13 descendants of its own

Source page: https://510kreport.com/device/K926501
Methodology: https://510kreport.com/methodology