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Cook Medical

 •  May 16

Flourish device illustration in pediatric anatomy Bloomington, Ind. – Cook Medical announced today that the U.S. Food and Drug Administration (FDA) has granted the Flourish™ Pediatric Esophageal Atresia device authorization under the Humanitarian Device Exemption (HDE) for the treatment of pediatric esophageal atresia. Esophageal atresia is a...

Cook Medical

 •  February 23

Universa® Percutaneous Drainage Catheters Bloomington, Ind.— Cook Medical has rounded out the Universa line with the introduction of two new sets for percutaneous urinary drainage. Each set includes a catheter and accessories for specific procedures. These sets streamline Cook’s offering of percutaneous drainage products. These Universa set...

Cook Medical

 •  November 15, 2016

BLOOMINGTON, Ind.– Cook Medical has completed enrollment in the first clinical study of an iliofemoral venous stent conducted in the United States under an FDA-approved Investigational Device Exemption (IDE). The VIVO Clinical Study is a prospective, non-randomized, multi-center study intended to evaluate the safety and effectiveness of the Zilver®...

Cook Medical

 •  August 12, 2016

FOR IMMEDIATE RELEASE: August 12, 2016
Cook Incorporated
750 Daniels Way, P.O. Box 489
Bloomington, Indiana 47402
1-812-339-2235
www.cookmedical.com Roadrunner® UniGlide® Hydrophilic Wire Guide DSM Biomedical B.V., the Netherlands, Cook Medical’s supplier of hydrophilic coating for the Roadrunner® Uniglide® Hydrophilic Wire Guide, recalled...

Cook Medical

 •  May 2, 2016

Cook Medical has initiated a global, voluntary recall of all catheters with Beacon® Tip technology. This recall includes all lots of catheters with the Beacon Tip technology. The catheters were recalled on April 15, 2016 due to complaints of tip splitting and/or fracture. The U.S. Food and Drug Administration (FDA) has not yet classified the...

Cook Medical

 •  March 3, 2016

Limerick, Ireland – In 2016 Cook Medical will celebrate 20 years of operations in the National Technology Park where it has grown from a primary team of less than a dozen people to a staff of over 800, who are designing and delivering life-changing devices every day. The medical device company provides minimally invasive technologies that are...

Cook Medical

 •  February 10, 2016

On January 6, 2016, Cook Medical initiated a voluntary recall of 360 specific lots of Single Lumen Central Venous Catheters and Pressure Monitoring Sets and Trays due to catheter tip fracture and/or separation. Globally, 17,827 devices are subject to this recall. The recalled products are specific versions and lot numbers of the Single Lumen...

Cook Medical

 •  February 1, 2016

West Lafayette, Ind. – MED Institute (MED) has been renamed as Cook Research Incorporated (CRI) and remains located in the Purdue Research Park at 1 Geddes Way in West Lafayette, Indiana. CRI supports Cook Medical in the identification, development, testing, and regulatory approval of innovative medical products. “Although Cook Research...

Cook Medical

 •  January 26, 2016

Bloomington, Ind. ─ In November, following the Food and Drug Administration approval of Cook Medical’s Zenith Alpha™ Thoracic Endovascular Graft, the first patient was treated with the device in the U.S.
Zenith Alpha Thoracic is indicated for the endovascular treatment of patients with isolated lesions of the descending thoracic aorta (not...

Cook Medical

 •  December 24, 2015

Bloomington, Ind. — Cook Medical applauds the successful efforts of legislators in both the U.S. Senate and House of Representatives last week to suspend the burdensome medical device excise tax for two years. This action to suspend the medical device tax will increase jobs in the device manufacturing industry and lift a financial burden from a...