Imris Imaging, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Imris Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InVision™ 3T Recharge Operating Suite
1
Total
1
Cleared
0
Denied
Imris Imaging, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chaska, US.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Imris Imaging, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Imris Imaging, Inc.
1 devices