MDR, MDSAP, and FDA audits demand rigorous preparation, lifecycle traceability, and risk-based compliance for global market ...

WORK Medical’s subsidiary Hunan Saitumofei receives manufacturing approval for its Class II medical devices: Hangzhou, China Wednesday, December 31, 2025, 15:00 Hrs [IST] WORK M ...

A new proposal in JAMA Internal Medicine suggests that the FDA should create an approval pathway for medical AI tools that parallels how physicians are trained and licensed.

GE HealthCare Technologies Inc. (NYSE: GEHC) leads with 100 FDA-approved AI devices, concentrating heavily on imaging and diagnostics. Their CleaRecon DL technology sharpens cone-beam CT images using ...

Positron Corporation (OTC: POSC) (the "Company"), a leading molecular imaging medical device company specializing in Positron Emission Tomography (PET) ...

Demand for Intuitive Surgical's da Vinci surgical robot is growing faster than the company's sales of new robots.

Companies to leverage and collaborate on research and development, distribution, and regulatory expertise to accelerate global adoption of intelligent testing technologies Alliance positions INBS to ...

The purpose of this research is to define the conditions under which developing countries find themselves implementing Artificial Intelligence in their governance systems. This scientific contribution ...

To do that, we must boldly go where no one has gone before... and have some craic along the way. Athbhliain faoi mhaise ...

While it’s probably safe to say that most people want to be rich, attaining wealth is far from easy. And yet, with ...

UTime Limited (Nasdaq: WTO), a global technology company engaged in the design and development of mobile devices today announced a major commercial breakthrough. UTime’s Hong Kong subsidiary, UTime ...

Here are 40 spine devices and technologies earning FDA clearances in 2025. Note: This is not an exhaustive list. 1. SurGenTec earned FDA 510(k) clearance for its OsteoFlo HydroFiber to be used as a ...