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Surgvision GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)March 20, 2024
K222240EXPLORER AIR® IIFebruary 28, 2023
K214097Explorer Air IIFebruary 25, 2022