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After successfully testing the hand-made device in the laboratory, Bakken returned to create a refined model for patients. However, much to his astonishment, when he came in the next day, he found the pacemaker already in use on a patient. (The Food and Drug Administration did not start regulating medical devices until 1976.) [4]
Medtronic plc is an American-Irish medical device company. The company's operational and executive headquarters are in Minneapolis, Minnesota, and its legal headquarters are in Ireland due to its acquisition of Irish-based Covidien in 2015.
Covidien (formerly an independent company known as Covidien plc) is an Irish-headquartered global health care products company and manufacturer of medical devices and supplies. Covidien became an independent publicly traded company after being spun off from Tyco International in 2007. [ 3 ]
Medtronic is expanding its products for endovascular aortic repair in the U.S. with two new devices: the FDA-approved Endurant II Aorto-Uni-Iliac (AUI) Stent Graft System and the FDA 510(k ...
Medtronic (NYS: MDT) announced Wednesday that it is offering a $2.5 million grant to Yale researchers who will independently review the safety of the company's controversial Infuse bone graft product.
Intersect ENT develops products for Ear, Nose and Throat conditions as well as the treatment of sinusitis. [2] Its most known device is the Propel mometasone furoate implant that is used after sinus surgery to keep the sinus passageways open and aid in the healing process by delivering an anti-inflammatory steroid directly to the sinuses.