The Food and Drug Administration has identified a Class I recall of Q’Apel Medical 072 Aspiration System after the company ...

The rise of AI in health care presents new challenges related to the patentability and regulation of AI-driven medical ...

COIMBATORE: The state government is set to establish the first Medical Devices Testing Laboratory in Coimbatore district for Rs 29.67 crore. However, sources sa ...

Q’Apel Medical announced that the FDA classified a voluntary recall of its 072 A System as Class I, the most serious kind.

On April 7, 2025, the U.S. Food and Drug Administration (“FDA” or “the agency”), classified Q’Apel Medical, Inc.’s (“Q’Apel” or “the company”) voluntary recall of 1,617 units of its 072 Aspiration ...

Short Summary The EU, UK, and USA each have distinct and evolving regulatory systems for medicines and medical devices, involving strict approval, surveillance, and market access requirements managed ...

Fremont, California Monday, April 21, 2025, 18:00 Hrs [IST] ...

“I really enjoyed my work. I loved the mission of trying to keep these medical devices safe for everybody who’s going to use them.” Classifications for reported “de novo” medical ...

(Yicai) April 24 -- The cost of US medical devices in China is set to rise significantly with the introduction of new tariffs ...