FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

AlignerFlow LC

K Number: K231817 · Decision Dec 1, 2023
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
119
Review Days
163

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Basic Information

Device Name
AlignerFlow LC
K Number
K231817
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3750
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Voco GmbH
Date Received
June 21, 2023
Decision Date
December 1, 2023
Product Code
DYH
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
DYH Adhesive, Bracket And Tooth Conditioner, Resin

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