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Cypris Medical

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K240185Cypris eXact Suture Placement DeviceMay 3, 2024
K233355Cypris eXact Suturing SystemJanuary 12, 2024