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

CLARITY MODIFIED CERAMIC BRACKETS

K Number: K062305 · Decision Oct 18, 2006
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
59
Applicant Total
6
Review Days
71

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Basic Information

Device Name
CLARITY MODIFIED CERAMIC BRACKETS
K Number
K062305
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5470
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
3M Unitek
Date Received
August 8, 2006
Decision Date
October 18, 2006
Product Code
NJM
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
NJM Bracket, Ceramic, Orthodontic

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K014142 UNITE BONDING ADHESIVE
K950514 TRI-CURE GLASS IONOMER ORTHODONTIC BAND CEMENT