Medical Device Manufacturer · US , San Diego , CA

The Argen Corporation - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2007

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

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