FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Invisalign® Palatal Expander System

K Number: K252931 · Decision Oct 23, 2025
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
143
Applicant Total
11
Review Days
38

Basic Information

Device Name
Invisalign® Palatal Expander System
K Number
K252931
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.5470
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Align Technology, Inc.
Date Received
September 15, 2025
Decision Date
October 23, 2025
Product Code
NXC
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NXC Aligner, Sequential

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Other Clearances by Align Technology, Inc.

K Number Device Name
K252870 Invisalign Specifix Attachment System
K252380 Invisalign System
K241412 Invisalign System
K232887 Invisalign Palatal Expander System
K232233 Invisalign System with Mandibular Advancement Featuring Occlusal Blocks
K222894 Invisalign System, Pre-Formed Attachment System
K220287 Invisalign System
K193659 iTero Element 5D
K181739 Invisalign System with Mandibular Advancement Feature
K143630 Invisalign System
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