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

ArgenIS Titanium Abutments

K Number: K172430 · Decision May 18, 2018
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
5
Review Days
280

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Basic Information

Device Name
ArgenIS Titanium Abutments
K Number
K172430
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Argen Corporation
Date Received
August 11, 2017
Decision Date
May 18, 2018
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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Other Clearances by Argen Corporation

K Number Device Name
K242458 ArgenZ MTZ
K192846 Argen Clear Aligner, Argen Clear Aligner Premium
K183229 Argen Clear Aligner
K160248 ArgenIS Titanium Abutments