Medien International Co, Ltd. is one of 19009 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medien International Co, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Galaxy R Digital Radiography Upgrade, GALAXY PLUS, DIGITAL RADIOGRAPHY SYSTEM, MODELS GALAXY 900 AND 1600
3
Total
3
Cleared
0
Denied
Medien International Co, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Echo, US.
Historical record: 3 cleared submissions from 2010 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Medien International Co, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Medien International Co, Ltd.
3 devices