Xanacare Technologies, LLC is one of 18984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xanacare Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: SimulCare II(TM), COMBOCARE 2000, COMBOCARE 2000
3
Total
3
Cleared
0
Denied
Xanacare Technologies, LLC has 3 FDA 510(k) cleared medical devices. Based in Golden, US.
Historical record: 3 cleared submissions from 2008 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Xanacare Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hart Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Xanacare Technologies, LLC
3 devices