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
5
Total
5
Cleared
0
Denied
Ventris Medical has 5 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Latest FDA clearance: Jul 2026. 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
5 devices
Cleared
Jul 02, 2026
Collagen Wound Powder
General & Plastic Surgery
128d
Cleared
Mar 21, 2025
Porous Biologic Scaffold
Orthopedic
24d
Cleared
Dec 18, 2024
Porous Biologic Scaffold
Orthopedic
273d
Cleared
Mar 07, 2024
Synthetic Bone Putty
Orthopedic
20d
Cleared
Sep 02, 2022
Synthetic Bone Putty
Orthopedic
88d