FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

ES BOND

K Number: K120767 · Decision May 24, 2012
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
17
Review Days
71

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Basic Information

Device Name
ES BOND
K Number
K120767
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spident Co., Ltd.
Date Received
March 14, 2012
Decision Date
May 24, 2012
Product Code
KLE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

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 Spident Co., Ltd.

K Number Device Name
K250566 EsCem RMGI
K250317 EsFlow PLUS
K242702 VioSeal
K242675 FineEtch (FineEtch-10 1.2ml, FineEtch-10 5ml, FineEtch-37 1.2ml FineEtch-37 5ml, FineEtch 37% 1.2ml 20ea pack)
K241445 K-Bond Universal
K231523 EsCom250
K214076 EsCem
K214071 Hexa-Temp
K161774 i-Sil
K134022 BASE IT
Search all 17 clearances from Spident Co., Ltd. →