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

FluoroDose Varnish

K Number: K250714 · Decision Nov 21, 2025
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
47
Review Days
256

Basic Information

Device Name
FluoroDose Varnish
K Number
K250714
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3260
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Centrix, Inc.
Date Received
March 10, 2025
Decision Date
November 21, 2025
Product Code
LBH
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
LBH Varnish, Cavity

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