FDA 510(k) FDA class 2 Substantially Equivalent 🇱🇮 Liechtenstein

Tetric PowerFill

K Number: K183380 · Decision Mar 14, 2019
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
31
Review Days
98

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Basic Information

Device Name
Tetric PowerFill
K Number
K183380
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ivoclar Vivadent, AG
Date Received
December 6, 2018
Decision Date
March 14, 2019
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

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K191448 Barrier Sleeves
K191382 IPS e.max CAD Abutment Solutions- extra systems
K190339 Helioseal F Plus
K190272 Bluephase PowerCure
K173573 Tetric CAD
K163613 Bluephase Style 20i
Search all 31 clearances from Ivoclar Vivadent, AG →