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

Telio CAD Abutment Solutions- extra systems

K Number: K193193 · Decision Nov 16, 2020
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
31
Review Days
363

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Basic Information

Device Name
Telio CAD Abutment Solutions- extra systems
K Number
K193193
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ivoclar Vivadent, AG
Date Received
November 19, 2019
Decision Date
November 16, 2020
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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