Eos Imaging, Inc. is one of 18542 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eos Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: sterEOS Workstation, STEREOS WORKSTATION
2
Total
2
Cleared
0
Denied
Eos Imaging, Inc. has 2 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.
Historical record: 2 cleared submissions from 2013 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Eos Imaging, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Eos Imaging, Inc.
2 devices