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FDA Cleared and CE Marked, Telescope Enters Global Market with Design Innovations to Enable Smooth Delivery of Coronary Stents and Balloons DUBLIN - May 16, 2019 - Medtronic plc (MDT), a global leader ...

Since the advent of TAVR, the patient with coronary disease and severe aortic stenosis has posed a clinical quandary for interventional cardiologists—now a new practical guide is offering some tips.

A PTCA balloon catheter is a device having a balloon at the tip that may be inflated or deflated while in place to open, widen, or close a route. These are employed in surgical procedures, with the ...

September 2, 2010 — The US Food and Drug Administration has granted 510(k) clearance for a next-generation catheter-based coronary imaging system (LipiScan IVUS; InfraReDx Inc) to help clinicians ...

Teleflex Inc. announced that the FDA has granted an expanded indication for its specialty catheters and coronary guidewires for use in PCI for chronic total occlusions. According to a company press ...

NATICK, Mass.--(BUSINESS WIRE)--Corindus Vascular Robotics, a leading developer of precision vascular robotics, today announced it has been granted Food and Drug Administration (FDA) conditional ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Back to Healio The FDA has designated Medtronic’s ...

Medtronic plc (NYSE:MDT) recently announced the launch of the Telescope guide extension catheter, which will provide backup support and access to distal lesions. This marks the med-tech major’s foray ...

DUBLIN, Oct. 09, 2019 (GLOBE NEWSWIRE) -- Medtronic plc (NYSE:MDT) today announced the U.S. Food and Drug Administration (FDA) has classified the company’s voluntary field action initiated in March ...

DUBLIN--(BUSINESS WIRE)--The "Diagnostic Coronary Catheter and Guidewire Market | US | Units Sold, Average Selling Prices, Product Pipeline, Forecasts | 2018-2024| MedCore" report has been added to ...

Dec. 3, 2004 --- The U.S. Food and Drug Administration (FDA) has approved a surgical tag system to minimize surgical errors with respect to patient, site, and procedure; a self-anchoring (barbed) ...