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

WILLI GELLER CREAPEARL

K Number: K010160 · Decision Mar 27, 2001
Classifications
1
FEI Numbers
99
Registration Numbers
99
Same Product Code
54
Applicant Total
17
Review Days
70

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Basic Information

Device Name
WILLI GELLER CREAPEARL
K Number
K010160
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3590
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jensen Industries, Inc.
Date Received
January 16, 2001
Decision Date
March 27, 2001
Product Code
ELM
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
ELM Denture, Plastic, Teeth

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K Number Device Name
K183408 Jensen Shade Effect Liquids
K142043 INSYNC ZR HIGH TRANSLUCENCY ZIRCONIA
K112806 JENSEN ZIRCONIA
K111743 THE INSYNC CERAMIC SYSTEM
K070114 CREATION CP-ZI PORCELAIN
K050838 THE LF-P CERAMIC SYSTEM
K043201 WILLI GELLER CREATION ZI PORCELAIN
K043221 WILLI GELLER CREATION CP PORCELAIN
K032267 R&D DESIGNATION AP-052-5
K022206 JENSEN GOLD FOIL
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