Medtronic won CE mark for the Affera Sphere-360 catheter and completed the first cases of the device in the Horizon 360 IDE ...

Intuitive Surgical receives FDA clearance for the da Vinci 5 robot to be used in cardiac procedures, reports 18% procedure ...

Woori IO plans to accelerate its noninvasive CGM launch after FDA announced relaxed wearable device regulations.

Michael “Mick” Farrell, chairman and CEO of Resmed, has begun his two-year term as the new chair of AdvaMed’s board of ...

Medtronic will invest $90M in Anteris Technologies for DurAVR TAVR device development, contingent on a $200M IPO.

According to a June 1996 article in MD+DI, two surveys that year had pegged increased investments in information technologies ...

This week's Medtech in a Minute features news about Boston Scientific and a potentially dangerous chemical used in IV bags ...

North Carolina becomes the second state to ban DEHP in medical devices, requiring IV bag manufacturers to phase out usage by 2030.

Click Therapeutics’ CEO discusses the first FDA-cleared depression app, migraine treatment breakthrough, and digital ...

At MD&M West, he will present “ The Needle Boom: Scaling Overmolded Needle Manufacturing for the At Home Care Revolution ,” ...

Industry consultant Michael Drues will discuss how medical device companies can better prepare for FDA inspections.

Medtronic CEO Geoff Martha shed some light on the company's M&A strategy this week at the J.P. Morgan Healthcare Conference.