# K972029: Bicon Dental Implants II Part Abutment System

- Pathway: 510(k) (Traditional)
- Applicant: Bicon, Inc.
- Decided: Aug 18, 1997 after 77 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K042971: Titan Dental Implant System (2005), 0 descendants of its own

## Indications for use
The Bicon Two Part Abutment is designed for use in the mandible or maxi}la for support of a terminal or intermediate crown for fixed bridgework or for a single tooth crown.

Source page: https://510kreport.com/device/K972029
Methodology: https://510kreport.com/methodology