# K043428: Reliadent Dental Implant System

- Pathway: 510(k) (Abbreviated)
- Applicant: Bioinfera, Inc.
- Decided: Jul 12, 2005 after 211 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- 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
Indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient's chewing function.

Source page: https://510kreport.com/device/K043428
Methodology: https://510kreport.com/methodology