Argentum International, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Argentum International, LLC - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Argentum International, LLC has 8 FDA 510(k) cleared medical devices. Based in Lakemont, US.
Historical record: 8 cleared submissions from 1998 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Argentum International, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Argentum International, LLC
8 devices
Cleared
Mar 19, 2007
SILVERLON DIRECT PRESSURE WOUND CLOSURE STRIP
General & Plastic Surgery
3037d
Cleared
Mar 19, 2007
SILVERLON ADHESIVE STRIP
General & Plastic Surgery
3037d
Cleared
Mar 19, 2007
SILVERLON DIRECT PRESSURE WOUND DRESSING
General & Plastic Surgery
3037d
Cleared
Jan 24, 2003
SILVERLON CONTACT WOUND DRESSING
General & Plastic Surgery
88d
Cleared
Jan 17, 2003
SILVERLON ADHESIVE STRIP
General & Plastic Surgery
81d
Cleared
Sep 24, 1999
SILVERLON WOUND PACKING STRIPS
General & Plastic Surgery
304d
Cleared
Feb 22, 1999
SILVERLON ISLAND DRESSING, SILVERLON ISLAND PAD
General & Plastic Surgery
90d
Cleared
Sep 25, 1998
SILVERLON CONTACT WOUND DRESSING
General & Plastic Surgery
169d