Microsoft is adding the ability to rename your user account to the Windows 11 Settings app, ported over from the legacy Control Panel.

Doctors say that identifying the right patients will be critical to the future of the field. Only time will tell, according to trialists.

A Food and Drug Administration advisory panel suggested Tuesday that the agency improve how it regulates pulse oximeters, calling for clearer labeling and more rigorous testing of the devices. The ...

A 15-person FDA Circulatory System Devices Panel has unanimously voted against Johnson & Johnson MedTech’s V-Wave Ventura interatrial shunt, creating a setback for the major medtech leader. The panel ...

Microsoft shifts another Windows 11 feature to Settings from the Control Panel — but I expect the latter will still be with ...

The Google Home app is getting an update with a home panel that allows users to better monitor home devices. This comes after Google announced the public rollout of the revamped version of its app.

Microsoft Teams rolls out a new Device settings hub on the web, replacing audio and video menus with a unified panel ...

Given the lack of information on their effectiveness and the unreasonable risks for illness or injury, spinal sphere devices should be regulated as Class 3 devices that require premarket approval (PMA ...

DEHP Poses Risk to Children | Cracking Hip Implants Recalled | Should FDA Ban These Devices? | Needle Destructor Needs 510(k) | Ortho Development Cited for MDR Failures | Cooper Companies Also Cited A ...

Please provide your email address to receive an email when new articles are posted on . The FDA’s Circulatory System Devices Panel advised that for a stent graft system to treat patients with ...

A health advisory committee recommended that Medicare consider measures such as time in range and safety data when making coverage decisions about diabetes devices. In a Tuesday meeting, the Medicare ...