Ventris Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ventris Medical - FDA 510(k) Cleared Devices
Recent clearances: Porous Biologic Scaffold, Porous Biologic Scaffold, Synthetic Bone Putty
4
Total
4
Cleared
0
Denied
Ventris Medical has 4 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Latest FDA clearance: Mar 2025. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ventris Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bruder Consulting & Venture Group as regulatory consultant.
FDA 510(k) Regulatory Record - Ventris Medical
4 devices