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Idev Technologies, Inc.

11 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
SUPERA VERITAS (K130591)Idev Technologies, Inc.2013-05-02
SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM (K122546)Idev Technologies, Inc.2012-12-07
SUPERA VERITAS(R) INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM (K111627)Idev Technologies, Inc.2012-08-21
SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY SYSTEMS (K111766)Idev Technologies, Inc.2011-10-19
SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM (K093893)Idev Technologies, Inc.2010-10-05
SUPERA INTERWOVEN SELF-EXPANDING BILIARY NITINOL STENT DELIVERY CATHETER, MODEL # S-04-040-120 (K071646)Idev Technologies, Inc.2008-01-31
SURESAVE TM SELF-EXPANDABLE NITINOL STENT AND PRECISION TM DELIVERY CATHETER-SS06120060 (K060557)Idev Technologies, Inc.2006-08-15
TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060 (K050926)Idev Technologies, Inc.2005-05-09
AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL10060060 (K041374)Idev Technologies, Inc.2005-03-02
TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050 (K033188)Idev Technologies, Inc.2003-11-19
AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL 10060060 (K030504)Idev Technologies, Inc.2003-09-16

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Every clearance here is in the API, with alerts when new ones post.