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Vygon USA

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243361NutrifitDecember 19, 2024
K212370Leaderflex Mini and Leaderflex NanoAugust 29, 2022
K181208Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL CatheterNovember 2, 2018
K172899Vygon PICCsFebruary 26, 2018