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

BracePaste Prime Plus

K Number: K261840 · Decision Jun 3, 2026
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
45
Review Days
1

Basic Information

Device Name
BracePaste Prime Plus
K Number
K261840
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3750
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
American Orthodontics
Date Received
June 2, 2026
Decision Date
June 3, 2026
Product Code
DYH
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

Classifications

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

Product Code Device Name
DYH Adhesive, Bracket And Tooth Conditioner, Resin

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