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/ LuxCreo, Inc.
LuxCreo, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K253365
LuxCreo Flexible Partial Denture Resin
November 25, 2025
K250343
LuxCreo Clear Aligner System
April 8, 2025
K230592
LuxCreo Dental Night Guard Resin
January 18, 2024
K212680
LuxCreo Clear Aligner System
May 31, 2022