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

SR VIVODENT S, SR ORTHOTYP S, SR ORTHOLINGUAL S

K Number: K132984 · Decision Jan 14, 2014
Classifications
1
FEI Numbers
99
Registration Numbers
99
Same Product Code
54
Applicant Total
65
Review Days
112

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Basic Information

Device Name
SR VIVODENT S, SR ORTHOTYP S, SR ORTHOLINGUAL S
K Number
K132984
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3590
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ivoclar Vivadent, Inc.
Date Received
September 24, 2013
Decision Date
January 14, 2014
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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