FDA 510(k) Applications Submitted by PreXion Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K190320 02/13/2019 PreXion3D Explorer PreXion Corporation
K221525 05/26/2022 PreXion3D Explorer PRO PreXion Corporation
K222150 07/20/2022 PreXion3D Expedition PreXion Corporation
K193329 12/02/2019 PreXion3D Explorer EX PreXion Corporation
K203784 12/28/2020 PreXion3D Explorer PRO PreXion Corporation
K181983 07/25/2018 PreXion 3D Excelsior PreXion Corporation
K173878 12/21/2017 PreXion3D Excelsior PreXion Corporation
K232166 07/21/2023 PreXion3D Expedition PreXion Corporation
K161881 07/08/2016 PreXion3D Excelsior PreXion Corporation


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