# K925777: Branemark System Estheticone Abutment Complete

- Pathway: 510(k) (Traditional)
- Applicant: Nobelpharma USA, Inc.
- Decided: Apr 14, 1993 after 149 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.
125 later devices descend from it; 4 cite it directly.
0 of 126 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
- K041655: Bio Plant System (Implants and Abutments) (2004), 91 descendants of its own
- K052369: Exfeel Implant System (2006), 84 descendants of its own
- K070562: EZ Plus Implant System (2007), 74 descendants of its own
- K110955: Anyridge Internal Implant System (2011), 43 descendants of its own
- K020617: Nsi Hexed and Non-Hexed Implant System (2002), 36 descendants of its own

Source page: https://510kreport.com/device/K925777
Methodology: https://510kreport.com/methodology