FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

RODIN 3D Resin SPLINT, Hard/Flex

K Number: K231793 · Decision Mar 26, 2024
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
70
Applicant Total
11
Review Days
280

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Basic Information

Device Name
RODIN 3D Resin SPLINT, Hard/Flex
K Number
K231793
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Belport Company, Inc., Gingi-Pak
Date Received
June 20, 2023
Decision Date
March 26, 2024
Product Code
MQC
Advisory Committee
Unknown
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
MQC Mouthguard, Prescription

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Other Clearances by Belport Company, Inc., Gingi-Pak

K Number Device Name
K260430 Porcelain Etch Gel
K251775 RODIN Cement
K250279 RC-SwiftPrep
K250222 SDF Pro
K240688 RODIN Titan 3D Resin
K231060 ProMin Dental Desensitizing Gel
K223365 RODIN Palette Naturalizing Kit
K211420 Stasis Gel
K211419 Gingi-Aid Gel
K200462 EtchPro Etching Gel
Search all 11 clearances from Belport Company, Inc., Gingi-Pak →