Idev Technologies, Inc. is one of 5218 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Idev Technologies, Inc. - FDA 510(k) Cleared Devices
11
Total
4
Cleared
0
Denied
Idev Technologies, Inc. has 4 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 4 cleared submissions from 2003 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Idev Technologies, Inc. Filter by specialty or product code using the sidebar.
Idev Technologies, Inc. — FDA 510(k) Products and Clearance History
11 devices
Cleared
May 02, 2013
SUPERA VERITAS
Gastroenterology & Urology
56d
Cleared
Dec 07, 2012
SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY...
Gastroenterology & Urology
108d
Cleared
Aug 21, 2012
SUPERA VERITAS(R) INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC...
Gastroenterology & Urology
438d
Cleared
Oct 19, 2011
SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY...
Gastroenterology & Urology
118d
Cleared
Oct 05, 2010
SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY...
Gastroenterology & Urology
291d
Cleared
Jan 31, 2008
SUPERA INTERWOVEN SELF-EXPANDING BILIARY NITINOL STENT DELIVERY CATHETER,...
Gastroenterology & Urology
227d
Cleared
Aug 15, 2006
SURESAVE TM SELF-EXPANDABLE NITINOL STENT AND PRECISION TM DELIVERY...
Gastroenterology & Urology
166d
Cleared
May 09, 2005
TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060
Cardiovascular
26d
Cleared
Mar 02, 2005
AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL10060060
Cardiovascular
282d
Cleared
Nov 19, 2003
TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050
Cardiovascular
49d
Cleared
Sep 16, 2003
AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL 10060060
Cardiovascular
209d