Last synced on 14 November 2025 at 11:06 pm

Fas Aligner System

Page Type
Cleared 510(K)
510(k) Number
K242929
510(k) Type
Traditional
Applicant
Xplora 3D Europe S.L
Country
Spain
FDA Decision
Substantially Equivalent
Decision Date
12/20/2024
Days to Decision
87 days
Submission Type
Summary

Fas Aligner System

Page Type
Cleared 510(K)
510(k) Number
K242929
510(k) Type
Traditional
Applicant
Xplora 3D Europe S.L
Country
Spain
FDA Decision
Substantially Equivalent
Decision Date
12/20/2024
Days to Decision
87 days
Submission Type
Summary