The Argen Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Argen Corporation - FDA 510(k) Cleared Devices
Recent clearances: ArgenZ HT+, ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer
6
Total
6
Cleared
0
Denied
The Argen Corporation has 6 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 6 cleared submissions from 2007 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by The Argen Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Argen Corporation
6 devices
Cleared
Apr 12, 2019
ArgenZ HT+
Dental
86d
Cleared
Feb 08, 2019
ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ...
Dental
122d
Cleared
Sep 16, 2015
ArgenIS Titanium Abutments
Dental
328d
Cleared
Jul 13, 2015
ArgenZ Esthetic Plus
Dental
98d
Cleared
Jul 31, 2014
ARGEN PMMA
Dental
114d
Cleared
Aug 15, 2007
ARGEN PEARL BRAND ZIRCONIA
Dental
86d