PathoCare Holdings has announced the receipt of a private third-party tender offer for the secondary purchase of shares from ...

Edwards Lifesciences has received the US Food and Drug Administration (FDA) approval for its SAPIEN M3 mitral valve ...

CellBxHealth’s new CEO, Peter Collins, plans to shift the company’s focal point away from the one-stop-shop research model to ...

Shape Memory Medical’s IMPEDE embolisation plug range has received CE mark as a Class III device under the European Union’s ...

Medical devices and related software solutions maker ZOLL has introduced its next-generation LifeVest wearable cardioverter ...

MARAbio Systems has commercially introduced a new blood test for identifying maternal autoantibody related autism.

A new survey by Asimily has identified that persistent visibility gaps and internal process breakdowns are among the top ...

Abbott has secured the US Food and Drug Administration (FDA) and CE Mark approval for its Amplatzer Piccolo Delivery System, ...

The FDA has granted 510(k) clearance to SleepRes’ KPAP-powered Kricket PAP device for the treatment of obstructive sleep ...

Denmark-based Curasight has dosed the first patient in the Phase I clinical trial of its uTREAT diagnostic platform, ...

In June 2025, the FDA published its final expectations for premarket submissions and post-market lifecycle obligations for medical device cybersecurity protocols under Section 524B of the Federal Food ...