Argen Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Argen Corporation - FDA 510(k) Cleared Devices
Recent clearances: ArgenZ MTZ, Argen Clear Aligner, Argen Clear Aligner Premium, Argen Clear Aligner
5
Total
5
Cleared
0
Denied
Argen Corporation has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.
Latest FDA clearance: Oct 2024. Active since 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Argen Corporation Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Qserve Group, Us, Inc., Sterngold Dental, LLC and Trisler Consulting (Dba).
FDA 510(k) Regulatory Record - Argen Corporation
5 devices