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Mindray’s journey is a testament to how thoughtful innovation can transform healthcare delivery. As the company continues to expand its footprint, it remains focused on empowering clinicians and improving patient...
For medical device manufacturers, securing FDA clearance is a milestone that marks the transition from innovation to real-world impact. Yet, over the past few years, that journey has become increasingly...
Orthopedic surgery has seen groundbreaking changes in recent years, with robotic-assisted joint replacement procedures becoming increasingly popular. From total knee arthroplasties to hip resurfacing, surgical robotics has ushered in a...
On June 3, 2025, the U.S. Food and Drug Administration (FDA) released updated guidance concerning the reprocessing of single-use medical devices (SUDs). The update clarifies and tightens expectations around how...
FDA’s Struggling AI Tool Raises Concerns for Medical Device Approval As artificial intelligence (AI) continues to influence industries from transportation to finance, healthcare regulators have also begun integrating AI into...
The recent workforce reductions at the Food and Drug Administration (FDA) have stirred concerns across the medical technology sector. While many are focused on how these layoffs might delay approvals...
In a move hailed by healthcare innovators and providers alike, U.S. Senators Mike Rounds (R-SD) and Martin Heinrich (D-NM) introduced the Health Tech Investment Act (S. 1399). The bipartisan bill aims...
Severe weather events—whether hurricanes, floods, snowstorms, or heatwaves—can cause devastating disruptions to healthcare systems. One of the most critical areas at risk during such emergencies is medical equipment. From diagnostic...
Imagine a resource where you can not only purchase the equipment you need but also sell or trade outdated models, get expert repairs, and arrange hassle-free logistics—all in one place.
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