LUXCREO INC.

FDA Device Registration & Listing · Chicago, IL, US · Registration 3016237718

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016237718
FEI Number
3016237718
Entity Name
LUXCREO INC.
City/State/Country
Chicago, IL, US
Establishment Address
350 W. Ontario Street Suite 700 Chicago,lL.60654, Chicago, IL 60654, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
LuxCreo Inc. (Owner Number: 10071055)
Owner / Operator Contact Address
350 W Ontario Street Suite700Chicago,lL.60654, Chicago, IL 60654, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K253365
PMA Number
N/A

All Registered Proprietary Names

LuxCreo Dental Night Guard Resin LuxCreo Clear Aligner System LuxCreo Dental Clear Aligner Resin LuxCreo Clear Retainer System LuxCreo Clear Aligner System LuxCreo Dental Night Guard Resin FPD Reisn

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EEA Plate, Base, Shellac Dental Class 1 872.6200 2021-11-19
NXC Aligner, Sequential Dental Class 2 872.5470 2025-04-11
DYT Maintainer, Space Preformed, Orthodontic Dental Class 1 872.5525 2020-04-20
NXC Aligner, Sequential Dental Class 2 872.5470 2023-03-21
KMY Positioner, Tooth, Preformed Dental Class 1 872.5525 2024-01-21
MQC Mouthguard, Prescription Unknown Class U N/A 2024-01-21
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2025-12-03

Official Correspondent

Tao Feng

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LuxCreo Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K800400 Dentsply Intl. MAXUM DENTURE RESIN 1980-03-12
K033020 Cmp Industries, LLC IMPAK ACRYLIC REPAIR RESIN LIQUID 2003-12-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016237718. Last updated year: 2026. Please use registration number 3016237718 when referencing this establishment in official correspondence.
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