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Ultrasight , Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K252235PVAD IQ SoftwareDecember 18, 2025
K251416UltraSight GuidanceDecember 17, 2025
K223347UltraSight AI GuidanceJuly 24, 2023