Curvebeam, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curvebeam, LLC - FDA 510(k) Cleared Devices
Recent clearances: HiRise (1040-230), HiRise, CubeVue
6
Total
6
Cleared
0
Denied
Curvebeam, LLC has 6 FDA 510(k) cleared medical devices. Based in Warrington, US.
Latest FDA clearance: Jul 2024. Active since 2012. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Curvebeam, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Curvebeam, LLC
6 devices