Last synced on 2 May 2025 at 11:05 pm

LuxCreo Clear Aligner System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250343
510(k) Type
Special
Applicant
LuxCreo Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2025
Days to Decision
61 days
Submission Type
Summary

LuxCreo Clear Aligner System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250343
510(k) Type
Special
Applicant
LuxCreo Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2025
Days to Decision
61 days
Submission Type
Summary