FDA's new medical device quality management rules align U.S. standards with global requirements and give inspectors new ...

For most implants and other high-risk devices brought to market, manufacturers do nothing more than file some paperwork and ...

A fault in J&J MedTech’s CEREPAK detachable coils, used in intracranial aneurysm embolisation procedures, has been associated ...

Researchers at the company are trying to understand their A.I. system’s mind—examining its neurons, running it through ...

TransMedics Group, Inc. ("TransMedics") (Nasdaq: TMDX), a medical technology company that is transforming organ transplant therapy for patients with end-stage lung, heart, and liver failure, today ...

TransMedics Group, Inc. ("TransMedics") (Nasdaq: TMDX), a medical technology company that is transforming organ transplant ...

The manufacturer has identified that certain Abiomed heart pumps with differential pressure sensors have the potential to ...

FDA escalates Johnson&Johnson brain coil recall to Class I after device failures linked to patient death and serious injuries ...

The FDA issued a notice to label a recall of Johnson & Johnson MedTech's Cerenovus unit's detachable coils as its most ...

Medline recalls blood culture kits with packaging defects that may compromise sterility; customers must quarantine affected lots and follow ...

Healthcare providers are advised to stop using the devices after a failure to detach was linked with four serious injuries ...

According to MarketsandMarkets™, the Electrosurgery Market is projected to grow from about USD 8.01 billion in 2026 to USD 11 ...