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

HKBOND 2006

K Number: K063062 · Decision Dec 1, 2006
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
145
Review Days
57

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Basic Information

Device Name
HKBOND 2006
K Number
K063062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Heraeus Kulzer, Inc.
Date Received
October 5, 2006
Decision Date
December 1, 2006
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 Heraeus Kulzer, Inc.

K Number Device Name
K091494 FLEXITIME FLOW
K060994 MONDIAL
K052543 HERACERAM ZIRKONIA
K043504 PALAIMPACT
K043295 VERSYO.DIRECT
K042878 FLEXITIME XTREME
K030052 OSTIM
K040859 HERACERAM PRESS
K040043 NDX-40 ALLOY
K033628 ARTIC
Search all 145 clearances from Heraeus Kulzer, Inc. →