# K061323: Modification to Reliadent Dental Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Bioinfera, Inc.
- Decided: May 23, 2007 after 377 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
Longest line of descent: 5 generations back to K925765 (1993). 30 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040807: Mis Dental Implant System, Mis - Implant Technologies, Ltd. (2004) Summary page 1.

## Most influential descendants
- K122664: Zuga Dental Implant System (2013), 1 descendant of its own
- K171197: Zuga Dental Implant System (2018), 0 descendants of its own

## Indications for use
For immediate or delayed surgical placement of a Dental implant in the anterior region and to allow immediate restoration (for cosmetic purposes).

Source page: https://510kreport.com/device/K061323
Methodology: https://510kreport.com/methodology