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

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

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

Neurable has completed a $35m Series A funding round to expedite the commercialisation of its patented compact brain-signal ...

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

Thought leaders, regulators and non-profits like The Pew Charitable Trusts are calling for US Congress and the FDA to close a loophole in regulation surrounding lab-developed tests. Stanford School of ...

It will potentially still take just under a decade for BCIs to reach market, but clinical trials are advancing quickly. Image credit: Getty Images/Malte Mueller. You can’t get very far in a science ...

While there are an estimated 500,000 medical devices on the European market, as of 2023, there were only 43 notified bodies with the power to perform conformity assessments, either on recertifying ...

For developing nations, perhaps the foremost principle driving sustainable economic success is diversification. Diversified economies are more resilient against downturns and less vulnerable to shock ...

The acquisition comes with the aim of acquiring Artelon’s portfolio of devices and expanding options available to Stryker’s foot and ankle and sports medicine specialist customers. Credit: ...

Neuralink is currently conducting the first-in-human PRIME study (NCT06429735) in the US. Credit: Shutterstock/Kemarrravv13. The US Food and Drug Administration (FDA ...