Last synced on 14 November 2025 at 11:06 pm

PreXion3D Explorer PRO

Page Type
Cleared 510(K)
510(k) Number
K221525
510(k) Type
Traditional
Applicant
PreXion Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
57 days
Submission Type
Summary

PreXion3D Explorer PRO

Page Type
Cleared 510(K)
510(k) Number
K221525
510(k) Type
Traditional
Applicant
PreXion Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
57 days
Submission Type
Summary