The adoption of the MIPI A-PHY standard in robotic and endoscopic surgery tools, as well as other medical devices, could ...

Analysis by Houlihan Lokey suggests that healthcare institutions are favouring medical equipment that readily fits in with their existing systems.

AI-powered medical devices are improving diagnosis and helping doctors detect diseases earlier with greater accuracy.Wearables and remote m ...

As of April 25, 2025, the U.S. has imposed tariffs on over 180 countries and territories. This includes a universal 10% baseline tariff while larger tariffs are in a 90-day “pause” period. The tariffs ...

Modern conveyance systems help medtech manufacturers achieve flexibility, compliance, and integration in smart factories.

On October 1, 2024, the Food and Drug Administration (FDA) marked a major milestone in medical device cybersecurity enforcement. This marks one year since the retracted Refuse to Accept (RTA) policy ...

Opinion: Medical device companies can create a competitive advantage by leveraging data to strengthen compliance programs and by ensuring effective oversight of quality and regulatory reporting ...

Despite intensive medtech industry lobbying to secure a carve-out from the Trump administration’s expansive tariffs on all countries, medical devices have been swept up in the tariff net. Why it ...

Medical device lobbyists called for more staffing transparency in user fee negotiations with the Food and Drug Administration. In a Feb. 4 meeting, medtech industry representatives proposed updates to ...

Americans cannot rely on the Food & Drug Administration (FDA) to guarantee that medical devices are safe, and a recent Government Accountability Office (GAO) report only strengthens that conclusion.