FDA 510(k) Applications Submitted by PAUL CASCONE

FDA 510(k) Number Submission Date Device Name Applicant
K160248 02/01/2016 ArgenIS Titanium Abutments Argen Corporation
K961211 03/28/1996 ARGELITE 52+ ARGEN PRECIOUS METALS, INC.
K071410 05/21/2007 ARGEN PEARL BRAND ZIRCONIA THE 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
K965216 12/30/1996 ARGI-SATIN OR OPTI0-STAR ARGEN PRECIOUS METALS, INC.


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