Viscus Biologics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Viscus Biologics, LLC - FDA 510(k) Cleared Devices
Recent clearances: FibermarX Radiopaque Tissue Marker
3
Total
3
Cleared
0
Denied
Viscus Biologics, LLC has 3 FDA 510(k) cleared medical devices. Based in Stillwater, US.
Historical record: 3 cleared submissions from 2015 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Viscus Biologics, 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 - Viscus Biologics, LLC
3 devices