Ford and Lincoln owners have a new recall to take seriously if there is an F-150, Explorer, Expedition, Aviator, or Navigator ...

A small orifice area on its own should not dissuade operators from offering the procedure as an option, a researcher says.

Real-world operators have been leaving patients with acceptable but still less-than-optimal results after transcatheter ...

Valgen Medtech announced today that it received CE mark approval for its DragonFly transcathteter mitral repair system.

Philips said Thursday it has received 510(k) clearance for a heart procedure visualization tool it developed with Edwards Lifesciences. The system, called EchoNavigator R5.0 with DeviceGuide, uses ...

DeviceGuide combines ultrasound and X-ray scans to build a 3D model of the patient’s heart and automatically tracks the trajectory of the Pascal Ace clip implant. (Philips) Philips has secured an FDA ...

Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for ...

The DeviceGuide in use with EchoNavigator. [Image courtesy of Philips] Philips (NYSE:PHG) announced today that it received FDA 510(k) clearance for its EchoNavigator R5.0 with DeviceGuide.

The National Transportation Safety Board released a preliminary report for its investigation into a Bucks County nursing home explosion that happened in December. The explosion killed two people, a ...

With December on the horizon and a cold snap hitting the UK last week, the heating is likely in use now in households across the UK. Now a plumbing expert has explained exactly when it should be used ...

Edwards Lifesciences Corp. ((EW)) announced an update on their ongoing clinical study. Take advantage of TipRanks Premium at 50% off! Unlock powerful investing tools, advanced data, and expert analyst ...