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LuxCreo, Inc.

FDA Regulatory Profile

LuxCreo, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 25, 2025.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253365LuxCreo Flexible Partial Denture ResinNovember 25, 2025
K250343LuxCreo Clear Aligner SystemApril 8, 2025
K230592LuxCreo Dental Night Guard ResinJanuary 18, 2024
K212680LuxCreo Clear Aligner SystemMay 31, 2022

FDA data resources