Xironetic, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xironetic, LLC - FDA 510(k) Cleared Devices
Recent clearances: IntraOp VSP Software Device
1
Total
1
Cleared
0
Denied
Xironetic, LLC has 1 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Xironetic, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Paladin Medical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Xironetic, LLC
1 devices