Medical Device Manufacturer · US , Houston , TX

Idev Technologies, Inc. - FDA 510(k) Cleared Devices

11 submissions · 4 cleared · Since 2003

Recent clearances: SUPERA VERITAS, SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM, SUPERA VERITAS(R) INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

11

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Idev Technologies, Inc. Cardiovascular ✕

4 devices

1-4 of 4

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