# K112746: Dioslimon Implant System

- Pathway: 510(k) (Special)
- Applicant: Dio Corporation
- Decided: Oct 21, 2011 after 30 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: 3 generations back to K051018 (2005). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080126: Dio Protem Implant System, Dio Department Dsi, Inc. (2008) Summary page 1.

## Indications for use
The DioSlimon Implant System is intended to load immediately in partially or fully edentulous mandibles and maxillae to serve as temporary support for provisional prosthetic device during the healing phase fo permanent endlosseous dental implants.

Source page: https://510kreport.com/device/K112746
Methodology: https://510kreport.com/methodology