In response, the U.S. Congress passed the Federal Food, Drug and Cosmetic Act of 1938, granting FDA with “premarket review” ...

Nerivio REN wearable, a noninvasive and drug-free device, is hoping to change the way to treat and prevent migraine headaches ...

In a groundbreaking advancement for the orthopedic device industry, Sawbones and Numalogics, Inc. are proud to announce that ...

Company Plans to Initiate Pivotal Study of Transformative Implant Technology Designed to Help Patients with Cartilage Damage ...

In a new course, students prepare for the FDA's ramped up security requirements for insulin pumps, pacemakers, and other ...

Analysts expect a negative impact on ResMed Inc. (RMD) after privately held pharmaceutical company and rival Apnimed, Inc.

The Food and Drug Administration has authorized more medical devices that incorporate artificial intelligence. Keep track of ...

The FDA announced it will limit access to Covid-19 vaccines going forward to people 65 and older and others at high risk of ...

"FDA clears Trax Surgical’s compression staple system for orthopaedic use" was originally created and published by Medical ...

The FDA cleared marketing for the first in vitro diagnostic device that tests blood to aid in diagnosing Alzheimer disease.

For instance, Boston Scientific in November 2019, announced the launch of two devices within the peripheral drug-eluting product portfolio during separate late-breaking clinical trial presentations at ...