It isn't necessarily easy to build a 'separates' hi-fi system, where every component (amplifier, speakers and at least one source) is housed in a separate box. You need space, a fair budget and the ...

Robert M. Califf, MD, MACC, commissioner of the U.S. Food and Drug Administration (FDA), will take the stage today to deliver the ACC.24 Eugene Braunwald Keynote focused on the need to revamp the ...

In a letter to FDA Deputy Commissioner for Human Foods Jim Jones released Wednesday, Democratic Sens. Richard Blumenthal (Conn.), Tina Smith (Minn.), Cory Booker (N.J.) and Dick Durbin (Ill.) ...

The U.S. FDA inspection of Unit-2, the API manufacturing facility of Apitoria Pharma in Jinnaram Mandal, Sanga Reddy district, conducted from September 23-27, had concluded with the regulator ...

The new indications, approved Tuesday by the FDA, make Ozempic the most broadly indicated drug in its class, with the largest set of specific medical conditions that it may be prescribed to treat.

Broccoli florets sold in Walmart stores across 20 states that were recalled over bacterial contamination fears have been given the U.S. Food and Drug Administration (FDA)'s highest risk level.

An audit released by the Inspector General of the U.S. Department of Health and Human Services, the parent organization of the Food and Drug Administration (FDA), is not a pleasant read. Let us turn ...

Instylla’s Tembo Embolic System [Image courtesy of Instylla] Instylla today said it has won FDA 510(k) clearance for its Tembo Embolic System. Bedford, Massachusetts-based Instylla said the ...

Over the past 30 years, peripheral vascular embolization has significantly expanded, now encompassing a wide range of applications, including the treatment of vascular malformations, uterine artery ...

January 28, 2025—Instylla, Inc., a developer of solutions for peripheral vascular embolotherapy, announced the FDA 510(k) clearance of the Tembo embolic system. According to the company, Tembo is a ...

It’s not clear if the changes are temporary or if the pages will be restored. When asked about the removed webpages, an FDA spokesperson directed MedTech Dive to contact the Department of Health and ...