Medtronic applied AI to its Reveal Line insertable cardiac monitor devices to help detect arrhythmias and reduce false alerts ...
Philips (NYSE:PHG) announced today that it launched its now FDA-cleared Zenition 90 motorized mobile C-arm system.
Merit Medical issued an urgent medical device recall notice related to specific products that contain plastic syringes made ...
The Steerant aortic guidewire. [Image from Medtronic] Medtronic (NYSE:MDT) today announced the launch of its Steerant aortic ...
Smiths Medical issued an urgent field safety notice to warn of a potential defect with some of its Bivona tracheostomy products.
Vapotherm announced today that it entered into a definitive merger agreement that will result in the company going private.
[Image courtesy of CardioFlow] MicroPort CardioFlow Medtech Corporation today announced that it received CE mark for its ...
Medtronic EVP and Global Regions President Rob ten Hoedt [Photo courtesy of Pixium Vision] Medtronic EVP and Global Regions ...
Medtronic "will reduce roles across our global workforce," the company said after MassDevice broke news of organization-wide ...
Venus Medtech announced that study investigators completed the first implant of its transcatheter pulmonic valve replacement ...
After Megadyne discontinued its pediatric patient return electrodes, the FDA says a recall of the electrodes is Class I.
The FDA says a recall of Teleflex (NYSE:TFX) intra-aortic balloon catheter kits is Class I, the most serious kind of recall.