CDRH and CBER Release Final Guidance for the Q-Submission Program and Draft Guidance for PreSTAR - On May 29, 2025, the U.S. Food ...

West Virginia Attorney General JB McCuskey issued a consumer alert Friday morning warning parents of certain vaping devices ...

Commenting on its court win, the AMP said at the time: “If it had been left in place, the FDA’s Final Rule would have classified LDTs as medical devices, creating unwarranted regulatory ...

The breadth of medical devices in terms of safety, it’s enormous. You have a pacemaker on one end and a tongue depressor on the other, and then FDA has to figure out a regulatory scheme that ...

The Trump Administration has effectively ended the Biden Administration's attempt to regulate lab-developed tests,” TD Cowen ...

the mindset driven by regulations and best practices has not permeated the industry. Manufacturers and healthcare organizations using devices are both responsible for these lapses. The FDA’s ...

A new FDA artificial intelligence tool designed to streamline medical device reviews is faltering in its early rollout stages, raising concerns for agency staff and ethics experts about its ...

The Food and Drug Administration (FDA) has urged the Department of Health (DOH) to approve the immediate suspension of an ...

Exhibit 2: FDA-authorized breakthrough devices by regulatory pathway and class Source: Authors’ analysis. Market-authorized breakthrough devices are publicly listed on the FDA website ...

However, the integration of AI into medical devices raises significant regulatory challenges. Ensuring that these ...

Under this law, medical device companies pay fees to the FDA for regulatory services, which gives them influence over the process, Redberg said. “The [device] companies dictate that the FDA ...