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

LITE ART

K Number: K101621 · Decision Aug 23, 2010
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
59
Review Days
75

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Basic Information

Device Name
LITE ART
K Number
K101621
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Shofu Dental Corp.
Date Received
June 9, 2010
Decision Date
August 23, 2010
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

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Other Clearances by Shofu Dental Corp.

K Number Device Name
K111855 HY-BOND RESIGLASS
K110235 BEAUTIBOND MULTI
K110252 BEAUTIBOND MULTI PR PLUS
K101603 BEAUTIFIL FLOW PLUS
K093559 VINTAGE MP
K082744 BEAUTIBOND
K080517 RESICEM
K080834 VINTAGE ART
K080068 BEAUTIFIL OPAQUER
K071742 BEAUTIFIL II
Search all 59 clearances from Shofu Dental Corp. →