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

SureSmile Aligner (ASSY500020)

K Number: K260722 · Decision Apr 15, 2026
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
143
Applicant Total
21
Review Days
41

Basic Information

Device Name
SureSmile Aligner (ASSY500020)
K Number
K260722
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5470
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona, Inc.
Date Received
March 5, 2026
Decision Date
April 15, 2026
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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