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

SDF Pro

K Number: K250222 · Decision May 7, 2025
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
7
Applicant Total
11
Review Days
100

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Basic Information

Device Name
SDF Pro
K Number
K250222
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3260
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Belport Company, Inc., Gingi-Pak
Date Received
January 27, 2025
Decision Date
May 7, 2025
Product Code
PHR
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
PHR Diammine Silver Fluoride Dental Hypersensitivity Varnish

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K231793 RODIN 3D Resin SPLINT, Hard/Flex
K223365 RODIN Palette Naturalizing Kit
K211420 Stasis Gel
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K200462 EtchPro Etching Gel
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