The FDA determined this week that Cordis’ recent recall of several versions of its Super Torque angiographic catheters meet the criteria of a Class I recall, a label reserved for those the ...

Separately, Cordis said it was recalling its line of LuSee TLC Steerable Guidewires, single-use disposable devices that assist in the precise positioning of angioplasty catheters within coronary ...

The FDA has identified Cordis’ recall of its angiographic catheter with radiopaque marker bands as Class I, the most serious type of recall. According to a press release from the FDA ...

After six years, Cardinal Health is dropping its Cordis medical device division, makers of cardiovascular catheters and diagnostic hardware, in a $1 billion deal with private equity firm Hellman ...

SAN FRANCISCO--(BUSINESS WIRE)--Cordis Corporation today announced EMPIRA™ and EMPIRA™ NC RX PTCA Dilatation Catheters have received 510(k) regulatory clearance for the treatment of coronary ...

FREMONT, Calif.--(BUSINESS WIRE)-- Cordis Corporation today announced it has received clearance from the Food and Drug Administration of its latest innovation in guiding catheters: the ADROIT TM 6F ...

Cordis will launch its latest innovation in guiding catheters: the ADROIT™ 6F Guiding Catheter**. The ADROIT TM Guiding Catheter incorporates important technological advances. The catheter has ...

The AVIATOR(TM) Plus draws on the innovative delivery technology of the AVIATOR(TM) Catheter, first launched by Cordis Endovascular in the United States in 2002. As with other Cordis Endovascular ...

In a sense, the workers are helping to save lives. The Cordis de Mexico plant makes catheters and stents used to treat various circulatory system problems for Cordis Corp., a Miami Lakes, Fla.-based ...