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

Bluephase PowerCure

K Number: K190272 · Decision Jul 3, 2019
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
31
Review Days
145

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Basic Information

Device Name
Bluephase PowerCure
K Number
K190272
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ivoclar Vivadent, AG
Date Received
February 8, 2019
Decision Date
July 3, 2019
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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K191448 Barrier Sleeves
K191382 IPS e.max CAD Abutment Solutions- extra systems
K190339 Helioseal F Plus
K183380 Tetric PowerFill
K173573 Tetric CAD
K163613 Bluephase Style 20i
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