# Medien International Co, Ltd.

- Location (FDA's records): Anyang-Si, KR
- FDA decisions: 3 (2010–2017): 3 510(k) clearances
- Product codes: MQB (2), KPR (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Imaging Dynamics Company, Ltd.: 2 (https://510kreport.com/company/imaging-dynamics)
- Atlaim Corporation: 1 (https://510kreport.com/company/atlaim)
- DRGEM Corporation: 1 (https://510kreport.com/company/drgem)

## Recent decisions
- K172435: Galaxy R Digital Radiography Upgrade (Oct 13, 2017)
- K132921: Galaxy Plus (Jan 17, 2014)
- K093816: Digital Radiography System, Models Galaxy 900 and 1600 (Oct 5, 2010)

Source page: https://510kreport.com/company/medien-international