Radialis, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Radialis, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Radialis PET Camera
1
Total
1
Cleared
0
Denied
Radialis, Inc. has 1 FDA 510(k) cleared medical devices. Based in Thunder Bay, CA.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Radialis, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beanstock Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Radialis, Inc.
1 devices