# Orion Corporation Soredex

- Location (FDA's records): Helsinki, FI
- FDA decisions: 4 (1988–1998): 4 510(k) clearances
- Product codes: EHD (1), MUH (1), KPR (1), IXK (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 7 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Orion Corp.: 1 (https://510kreport.com/company/orion)
- Applicare Medical Imaging, B.V.: 1 (https://510kreport.com/company/applicare-medical-imaging)

## Firms that cite its devices most
- Soredex Palodex Group OY: 2 (https://510kreport.com/company/soredex-palodex-group)
- Cruxell Corp.: 1 (https://510kreport.com/company/cruxell)
- Afp Imaging Corp.: 1 (https://510kreport.com/company/afp-imaging)
- Denoptix, Inc.: 1 (https://510kreport.com/company/denoptix)
- Digident, Ltd.: 1 (https://510kreport.com/company/digident)

## Its most-cited devices
- K934949: Digora (1994), cited by 5
- K983267: Digora for Windows 2.0 (1998), cited by 1
- K880982: Oralix Pan DC Iii Ceph or Panoramic Mode Only (1988), cited by 1

## Recent decisions
- K983267: Digora for Windows 2.0 (Dec 30, 1998)
- K974877: Cranex Tome Ceph, or Cranex Tome (Mar 27, 1998)
- K934949: Digora (Feb 10, 1994)
- K880982: Oralix Pan DC Iii Ceph or Panoramic Mode Only (Jun 6, 1988)

Source page: https://510kreport.com/company/orion-soredex