# K193623: DIOnavi-Denture

- Pathway: 510(k) (Traditional)
- Applicant: Dio Corporation
- Decided: Oct 22, 2020 after 301 days
- Product code: EBI (Resin, Denture, Relining, Repairing, Rebasing)
- Device class: 2
- Regulation: 21 CFR 872.3760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K162044 (2017). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162044: Dentca Denture Base II, Dentca, Inc. (2017) Summary page 4.

## Most influential descendants
- K210828: DIOnavi-Denture02 (2021), 0 descendants of its own

## Indications for use
DIOnavi-Denture is a light-curable resin indicated for fabrication and repair of full and partial removable dentures and baseplates. The material is an alternative to traditional heat-curable and auto polymerizing resins. Fabrication of dental prosthetics with DIOnavi-Denture requires a computer-aided design and manufacturing (CAD/CAM) system that includes the following components: digital denture base files based on a digital impression, a digital light processing (DLP) printer, and curing light equipment.

Source page: https://510kreport.com/device/K193623
Methodology: https://510kreport.com/methodology