Ventris Medical

FDA Regulatory Profile

Ventris Medical appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 2, 2026.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260596Collagen Wound PowderJuly 2, 2026
K250556Porous Biologic ScaffoldMarch 21, 2025
K240765Porous Biologic ScaffoldDecember 18, 2024
K240458Synthetic Bone PuttyMarch 7, 2024
K221644Synthetic Bone PuttySeptember 2, 2022