Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact