Radiadyne, LLC is one of 21940 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radiadyne, LLC - FDA 510(k) Cleared Devices
Recent clearances: OARtrac System with Patient Specific Reusable Universal PSD Sensors, OARtrac System with Skin Sensors
2
Total
2
Cleared
0
Denied
Radiadyne, LLC has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Radiadyne, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Group as regulatory consultant.
FDA 510(k) Regulatory Record - Radiadyne, LLC
2 devices