# K203116: SensorX

- Pathway: 510(k) (Traditional)
- Applicant: Durr Dental SE
- Decided: Mar 19, 2021 after 154 days
- Product code: MUH (System, X-Ray, Extraoral Source, Digital)
- 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: 5 generations back to K933455 (1994). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K172918: DEXIS Titanium, KaVo IXS HD (Size 1, Size 2), Kavo Dental Technologies, LLC (2017) Summary page 5.

## Indications for use
The intraoral sensor is intended to convert x-ray photons into electronic impulses that may be stored, viewed and manipulated for diagnostic use by dentists.

Source page: https://510kreport.com/device/K203116
Methodology: https://510kreport.com/methodology