# K112380: Clearvision

- Pathway: 510(k) (Traditional)
- Applicant: Midmark Corp.
- Decided: Nov 22, 2011 after 97 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: 4 generations back to K933455 (1994). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072134: Schick Computed Oral Radiology System, Schick Technologies, Inc. (2007) Summary page 1.
- K090458: Dexis Sensor, Dexis, LLC (2009) Summary page 1.

## Indications for use
ClearVision is intended to be used by dentists and other qualified professionals for producing diagnostic x-ray radiographs of dentition, jaws and other oral structures.

Source page: https://510kreport.com/device/K112380
Methodology: https://510kreport.com/methodology