Winprobe Corporation

FDA Regulatory Profile

Winprobe Corporation has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Nov 7, 2017

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K173265UltraVision 2 Diagnostic Ultrasound SystemNov 7, 2017
K150580UltraVision 2 Diagnostic Ultrasound SystemApr 7, 2015