Venocare, Inc. is one of 16749 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Venocare, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ruby Intravascular Catheter, Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG), Ruby Intravascular Catheter
3
Total
3
Cleared
0
Denied
Venocare, Inc. has 3 FDA 510(k) cleared medical devices. Based in Doral, US.
Latest FDA clearance: Sep 2026. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Venocare, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Daniel & Daniel, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Venocare, Inc.
3 devices