Eyas Medical Imaging, Inc. has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Ascent 3T™ Neonatal Magnetic Resonance Imaging (MRI) System, a whole-body magnetic resonance ...

Zimmer Biomet’s G7 TM Acetabular System, an implant for primary and revision hip replacement surgeries, has received FDA 510(k) clearance. The system combines trabecular metal technology, an ...

February 4, 2026—Avantec Vascular, a Nipro company, announced FDA 510(k) clearance of its thrombectomy system, which is intended for the treatment of thrombus in the peripheral venous system.

Quanterix Corporation (Nasdaq: QTRX), a company transforming healthcare by accelerating biomarker breakthroughs from discovery to diagnostics, today announced it has submitted a 510(k) premarket ...

Company anticipates full data analysis by the end of March 2026; data to be incorporated into FDA 510(k) submission package NEW YORK, Jan. 28, 2026 (GLOBE NEWSWIRE) -- Intelligent Bio Solutions Inc.

Keurig is recalling over 80,000 K-Cup products due to possible mislabeling. Caffeinated coffee pods may have accidentally been labeled as decaf. Here’s a list of impacted products. If you find ...

Accelerate your tech game Paid Content How the New Space Race Will Drive Innovation How the metaverse will change the future of work and society Managing the ...

The updated eMurmur software expands compatibility from just one digital stethoscope model to more and introduces a new feature. [Photo courtesy of eMurmur] eMurmur has received FDA 510(k) clearance ...

The U.S. Food and Drug Administration (FDA) announced a voluntary recall of more than 80,000 McCafé Premium Roast Decaf Coffee K-Cup pods sold by Keurig Dr Pepper after the company found the pods ...

Keurig has issued a voluntary recall of one of its popular K-Cup varieties. The brand, known for its coffee makers and drink pods, shared details about the ongoing recall in a notice that was posted ...