510(k) K253365

Device
LuxCreo Flexible Partial Denture Resin
Applicant
LuxCreo, Inc.
510(k) number
K253365
Product code
EBI
Decision
Substantially Equivalent (SESE)
Decision date
2025-11-25
Date received
2025-09-30
Regulation
872.3760
Classification name
Resin, Denture, Relining, Repairing, Rebasing
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Tao Feng
Address
350 W. Ontario St., Suite 700 Chicago IL US 60654 60654

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00860013903138LuxCreoLuxcreo Inc2025-12-11
00860013903121LuxCreoLuxcreo Inc2025-12-11

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