Vault Paragon Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vault Paragon Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VaporShield, PowerPAK Syringe
2
Total
2
Cleared
0
Denied
Vault Paragon Group, Inc. has 2 FDA 510(k) cleared medical devices. Based in Oakland, US.
Latest FDA clearance: Dec 2025. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Vault Paragon Group, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vault Paragon Group, Inc.
2 devices