LuxDesign— 510(k) K260421
Substantially EquivalentLuxCreo, Inc.
FDA 510(k) clearance K260421 for LuxDesign, Substantially Equivalent on 2026-10-23. Applicant: LuxCreo, Inc.. Device class: 2.
Clearance details
- Applicant
- LuxCreo, Inc.
- Product code
- Product code PNN
- Device class
- Class 2
- Regulation
- 21 CFR 872.5470
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
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