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Eyas Medical Imaging Inc. has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Ascent3T Neonatal Magnetic Resonance Imaging (MRI) System, a whole-body magnetic resonance scanner designed and optimized specifically for neonate and infant anatomy, including head, body and extremities.

It is with profound sadness that we announce the passing of MEDITECH Founder and Chairman, A. Neil Pappalardo, on January 27, 2026 at the age of 83. After founding the company on August 4, 1969, Mr. Pappalardo remained a guiding force and driving inspiration until his passing, establishing a legacy that spans over five decades.

AIS has announced the addition of Chris Sheets and Andrew Long to the AIS team. Both joined AIS earlier this year as nuclear medicine field service engineers and “are already making valuable contributions to our growing service organization,” according to CEO Grant Norris.

Siemens Healthineers has received Food and Drug Administration clearance for the Biograph One, its second-generation positron emission tomography/magnetic resonance (PET/MR) scanner that enables simultaneous visualization of organ location, function and cellular metabolism.

The FDA’s Center for Devices and Radiological Health’s (CDRH) mission is to protect and promote public health while supporting timely access to innovative, safe and effective medical devices and safe radiation-emitting products.