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Prexion Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232166PreXion3D ExpeditionSeptember 8, 2023
K222150PreXion3D ExpeditionJanuary 12, 2023
K221525PreXion3D Explorer PROJuly 22, 2022
K203784PreXion3D Explorer PROFebruary 23, 2021
K193329PreXion3D Explorer EXApril 9, 2020
K190320PreXion3D ExplorerApril 15, 2019
K181983PreXion 3D ExcelsiorAugust 17, 2018
K173878PreXion3D ExcelsiorJanuary 19, 2018
K161881PreXion3D ExcelsiorOctober 3, 2016