# K023705: Bicon Transitional Implant (Bti) System

- Pathway: 510(k) (Traditional)
- Applicant: Bicon, Inc.
- Decided: Jan 29, 2003 after 86 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K073645: Simpler Mini Dental Implant: SM 3002 2.5 X 10MM, SM 3003 2.5 X 13MM, SM 3004 2.5 X 15MM (2008), 3 descendants of its own
- K083886: Simpler Mini Implant, Models SM 5002, SM 5003, SM 5004 (2009), 2 descendants of its own
- K121281: Simpli Simpler Implant System (2013), 0 descendants of its own
- K092674: Simpler Toadstool Mini Implant (2009), 0 descendants of its own

## Indications for use
The BTI System will be used to provide immediate or interim stability for new/existing dental prosthetics in partially or fully edentulous jaws.

Source page: https://510kreport.com/device/K023705
Methodology: https://510kreport.com/methodology