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Home
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Ventris Medical
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K250556
Porous Biologic Scaffold
March 21, 2025
K240765
Porous Biologic Scaffold
December 18, 2024
K240458
Synthetic Bone Putty
March 7, 2024
K221644
Synthetic Bone Putty
September 2, 2022