# K130109: Endograph DC

- Pathway: 510(k) (Abbreviated)
- Applicant: Villa Sistemi Medicali S.P.A.
- Decided: Aug 1, 2013 after 197 days
- Product code: EHD (Unit, X-Ray, Extraoral With Timer)
- Device class: 2
- Regulation: 21 CFR 872.1800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K935046 (1994). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120318: Vivi Ergon-X HF, Vivi S.R.L. (2012) Summary page 1.

## Most influential descendants
- K231055: x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology) (2023), 0 descendants of its own

## Indications for use
Endograph DC is an extracral source x-ray unit for dental radiographic examination and diagnosis of diseases of the teeth, jaw, and oral structures. The device is to be operated and used by dentists, radiologists and other legally qualified health care professionals. It can be used with both pediatric and adult patients.

Source page: https://510kreport.com/device/K130109
Methodology: https://510kreport.com/methodology