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Viasonix , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K242662Falcon/Xpress (Falcon/Xpress)December 18, 2024
K202742Dolphin/IQ, Dolphin/4D and Dolphin/MAX with Dolphin/XF robot accessoryJanuary 25, 2021
K192607LiteWalkDecember 19, 2019
K191023Dolphin/IQ, Dolphin/4D and Dolphin/MAXMay 16, 2019
K170859Dolphin/IQ and Dolphin/4DNovember 14, 2017
K111416FALCONJuly 15, 2011