Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1582585309
Device Listing 1582585309
Listing Summary
#
Listing key
1582585309
Premarket submission
K250343
Device
LuxCreo Clear Aligner System
Applicant
LuxCreo, Inc.
Product code
NXC
Decision date
2025-04-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
259890
3016237718
3016237718
LUXCREO INC.
1
N
2026-01-01
350 W. Ontario Street Suite 700 Chicago,lL.60654 Chicago IL US 60654