# K063459: Cranex Novus

- Pathway: 510(k) (Traditional)
- Applicant: Soredex Palodex Group OY
- Decided: Dec 26, 2006 after 41 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: 3 generations back to K972312 (1997). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043307: Cranex D, Soredex Palodex Group OY (2004) Summary page 1.

## Most influential descendants
- K092591: Orthopantomograph OP30 (2009), 0 descendants of its own

## Indications for use
The Cranex Novus dental panoramic equipment is indicated for dental radiographic examinations by producing digital radiographs of dentition, TM-joints and other oral structures.

Source page: https://510kreport.com/device/K063459
Methodology: https://510kreport.com/methodology