# K170733: ScanX Intraoral View

- Pathway: 510(k) (Traditional)
- Applicant: Duerr Dental AG
- Decided: May 1, 2017 after 52 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 K934949 (1994). 5 ancestors in all.
5 later devices descend from it; 3 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160788: RIOScan (RPS500), Ray Co., Ltd. (2016) Summary page 6.

## Most influential descendants
- K212080: Imaging Plate Scanner, i-Scan (2021), 1 descendant of its own
- K202633: ScanX Edge (2020), 1 descendant of its own
- K231660: Digital image scanner of dental (2023), 0 descendants of its own
- K230095: ScanX Swift 2.0, ScanX Swift View 2.0 (2023), 0 descendants of its own
- K191623: ScanX Touch/ScanX Duo Touch (2019), 0 descendants of its own

## Indications for use
The ScanX Intraoral View is intended to be used for scanning and processing digital images exposed on Phosphor Storage Plates (PSPs) in dental applications.

Source page: https://510kreport.com/device/K170733
Methodology: https://510kreport.com/methodology