Flexible Stenting Solutions, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Flexible Stenting Solutions, Inc. - FDA 510(k) Cleared Devices
5
Total
0
Cleared
0
Denied
Flexible Stenting Solutions, Inc. has 0 FDA 510(k) cleared medical devices. Based in Eatontown, US.
Historical record: 0 cleared submissions from 2009 to 2012. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Flexible Stenting Solutions, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Flexible Stenting Solutions, Inc.
5 devices
Cleared
Jul 06, 2012
FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM
Gastroenterology & Urology
84d
Cleared
Apr 24, 2012
FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM
Gastroenterology & Urology
70d
Cleared
Dec 30, 2011
FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM
Gastroenterology & Urology
121d
Cleared
Nov 22, 2010
FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BX
Gastroenterology & Urology
81d
Cleared
Sep 15, 2009
FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM
Gastroenterology & Urology
428d