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FDA 510(k) Applications Submitted by Argen Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160248
02/01/2016
ArgenIS Titanium Abutments
Argen Corporation
K172430
08/11/2017
ArgenIS Titanium Abutments
Argen Corporation
K192846
10/03/2019
Argen Clear Aligner, Argen Clear Aligner Premium
Argen Corporation
K183229
11/20/2018
Argen Clear Aligner
Argen Corporation
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