FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

DENTOETCH QUICKBOND BOND ACTIVATOR

K Number: K122522 · Decision Mar 19, 2013
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
8
Review Days
211

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Basic Information

Device Name
DENTOETCH QUICKBOND BOND ACTIVATOR
K Number
K122522
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Itena Clinical
Date Received
August 20, 2012
Decision Date
March 19, 2013
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

Other 510(k) clearances with the same product code (KLE), ordered by most recent decision date.

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Other Clearances by Itena Clinical

K Number Device Name
K170207 Obturys
K162960 TotalC-Ram
K122551 PROVITEMP
K122521 PREVENT SEAL
K122549 DENTO TEMP
K121804 PROVITEMP, DENTOTEMP, TOTALCEM, DENTOCEM
K121769 DENTOCORE / DENTOCORE BODY