# K062044: The 5.0 X 6.0MM Dental Implant

- Pathway: 510(k) (Traditional)
- Applicant: Bicon, Inc.
- Decided: Nov 21, 2006 after 125 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.
5 later devices descend from it; 3 cite it directly.
0 of 6 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
- K150571: 3i T3 Short Implants (2015), 1 descendant of its own
- K103810: KJ Submerged System (2011), 1 descendant of its own
- K241753: Immediate Molar Implants (2024), 0 descendants of its own
- K202046: LOTA SLA Dental Implant System and LOTA HA Dental Implant System (2022), 0 descendants of its own
- K122198: 6.00MM X 6.00MM Macro External Implant System (2013), 0 descendants of its own

## Indications for use
The 5.0 x 6.0mm locking-taper Bicon dental implant is intended to be surgically placed in the maxilla or mandible to provide support for prosthetic devices to restore the patient's chewing function.

Source page: https://510kreport.com/device/K062044
Methodology: https://510kreport.com/methodology