Technology

February 16, 2012 — Siemens Healthcare received clearance from the U.S. Food and Drug Administration (FDA) for syngo Aortic ValveGuide, an integrated image processing software that helps cardiologists and cardiac surgeons prepare and perform transcatheter aortic valve replacement (TAVR).

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February 16, 2012 — Velomedix Inc., a clinical stage medical device company, announced it has received investigational device exemption (IDE) approval from the U.S. Food and Drug Administration (FDA) to evaluate the use of rapid therapeutic hypothermia for the treatment of patients suffering an acute myocardial infarction (AMI or heart attack).

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February 16, 2012 — Aptus Endosystems, a company developing advanced technology for endovascular aneurysm repair (EVAR), announced the start of ANCHOR; a global, multicenter, prospective post-market registry evaluating the use of the HeliFX aortic securement system in the treatment of aortic aneurysms.

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February 15, 2012 — Vessix Vascular Inc., developer of a novel percutaneous radiofrequency (RF) balloon catheter technology, announced that it will make its first detailed public presentation of preclinical data relating to its new V2 Renal Denervation System on Saturday, Feb. 18, 2012 at the TRenD Workshop 2012, in Frankfurt, Germany.

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February 15, 2012 — CardioNet Inc. a wireless medical technology company announced the acquisition of ECG Scanning and Medical Services Inc.

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February 15, 2012 — Medtronic Inc. announced the start of two clinical initiatives evaluating the broader, real-world clinical use of the company’s Symplicity renal denervation system across multiple conditions.

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February 14, 2012 — The American College of Radiology (ACR) called on Congress to reject what would be the eighth cut to Medicare funding for imaging scans in the last six years and protect the ability of seniors to receive this live-saving care.

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February 10, 2012 — Researchers from the National Institute of Advanced Industrial Science and Technology (AIST), Japan, determined arterial stiffness using the relationship between cuff pressure and arterial volume.

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February 10, 2012—Merit Medical Systems recently announced it acquired the assets of Ostial Solutions LLC, maker of the Ostial Pro stent positioning system.

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February 9, 2012 — The U.S. Food and Drug Administration (FDA) sent a warning letter to Merit Medical Systems Inc. regarding modifications to the hydrophilic coating process for the Merit Laureate Hydrophilic Guidewire, following an inspection of the company's facility in Galway, Ireland.

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February 9, 2012 — Stereotaxis Inc. said its Vdrive robotic navigation system, which provides physicians the ability to remotely manipulate traditionally non-robotic catheters, is growing in popularity and is expected to surpass 500 clinical procedures in Europe in February.

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February 9, 2012 — Boston Scientific announced the United States launch of the TruePath CTO device, designed to facilitate the crossing of chronic total occlusions (CTOs, or complete blockages) within the peripheral vasculature.

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St. Jude Medical has launched its Unify Quadra cardiac resynchronization therapy defibrillator (CRT-D) and Quartet left ventricular quadripolar pacing lead. It features four electrodes spaced over 4.7 cm, enabling up to 10 pacing configurations for better cardiac rhythm management.

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February 9, 2012 — Healthcare imaging specialist Barco announced that it has signed an agreement to acquire U.K.-based JAOtech, a manufacturer of patient entertainment and point-of-care terminals for hospitals.

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February 9, 2012 — Valley Presbyterian Hospital (VPH) was the site for the first implantation in the United States of a new heart device since the U.S. Food and Drug Administration (FDA) approved the DF4 High-Voltage Connector System by Medtronic earlier this month, Gus Valdespino, VPH president and CEO announced.

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