# K220556: OpenSensorX Series

- Pathway: 510(k) (Special)
- Applicant: Dentimax, Inc.
- Decided: Apr 13, 2022 after 44 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: 2 generations back to K050693 (2005). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092547: Dentimax Digital X-Ray Imaging System Sensor Size 1, 2, Dentimax Usb Control Box, Dentimax (2009) Summary page 4.

## Indications for use
The OpenSensorX Series is used in conjunction with dental Radiography in medical units. The product is used for dental X-ray examination and the diagnosis of structural diseases. The product is expected to be used in hospitals and clinics, operated and used by trained professionals under the guidance of doctors. This device is not intended for mammography and conventional photography applications. This device is suitable for providing dental radiography imaging for both adult and pediatric.

Source page: https://510kreport.com/device/K220556
Methodology: https://510kreport.com/methodology