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

SIMILE FLOW

K Number: K052106 · Decision Oct 31, 2005
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
13
Review Days
89

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Basic Information

Device Name
SIMILE FLOW
K Number
K052106
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pentron Clinical Technologies
Date Received
August 3, 2005
Decision Date
October 31, 2005
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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K071500 NANO-BOND II ADHESIVE SYSTEM
K060889 SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE
K060698 CEMENT-IT ALL PURPOSE, MODEL N97
K052349 AVANTE LED CURING UNIT, MODEL N44
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