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

AVANTE CURELIGHT

K Number: K003683 · Decision Jan 11, 2001
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
211
Applicant Total
78
Review Days
43

Basic Information

Device Name
AVANTE CURELIGHT
K Number
K003683
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
JENERIC/PENTRON, INC.
Date Received
November 29, 2000
Decision Date
January 11, 2001
Product Code
EBZ
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
EBZ Activator, Ultraviolet, For Polymerization

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Other Clearances by JENERIC/PENTRON, INC.

K Number Device Name
K020499 BOND-3 ADHESIVE
K013543 BOND-1 C & B
K013542 DENTIN CONDITIONING AND ADHESIVE SYSTEM (BOND-1)
K012231 AVANTE MICRO CRYSTAL SYSTEM
K011748 FIRST FILL R.C.S.
K010957 QUELL DESENSITIZER
K011331 JP CAST 40
K011330 JP CAST 50
K011362 GOLD CORE 73 LS
K010044 COSMIC
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