Biovision Technologies, LLC is one of 18961 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biovision Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: NeedleCam HD Visualization System, NEEDLE VIEW CH SCOPE KITS, SURGVIEW INTEGRATED VISUALIZATION SYSTEM
3
Total
3
Cleared
0
Denied
Biovision Technologies, LLC has 3 FDA 510(k) cleared medical devices. Based in Golden, US.
Historical record: 3 cleared submissions from 2008 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Biovision Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biovision Technologies, LLC
3 devices