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

GENERATION 8 SE ADHESIVE

K Number: K072480 · Decision Nov 21, 2007
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
13
Review Days
78

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Basic Information

Device Name
GENERATION 8 SE ADHESIVE
K Number
K072480
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pentron Clinical Technologies
Date Received
September 4, 2007
Decision Date
November 21, 2007
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

Similar 510(k) Clearances

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Other Clearances by Pentron Clinical Technologies

K Number Device Name
K091512 BUILD-IT LIGHT CURE
K081887 LUTE-IT II VENEER CEMENT, MODEL NO6
K072830 RM BOND, MODEL J032
K072545 ARTISTE SE FLOWABLE COMPOSITE, MODEL N280
K071500 NANO-BOND II ADHESIVE SYSTEM
K060889 SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE
K060698 CEMENT-IT ALL PURPOSE, MODEL N97
K052106 SIMILE FLOW
K052349 AVANTE LED CURING UNIT, MODEL N44
K023818 FIBERFILL AGP
Search all 13 clearances from Pentron Clinical Technologies →