Clinicians use the device to image blood flow dynamics during retinal exams, helping them spot age-related macular degeneration, diabetic retinopathy, and retinal vein occlusions.

As of June 1, 33 medical device reports have been identified, including 22 device malfunctions and 11 related to injuries.

The U.S. Food and Drug Administration recently announced its latest emergency use authorization.

A lack of consistency in policies around the country in 2020 invites the question: Do residency program directors need national guidelines on parental leave?

Chief executive William Thorwarth Jr., MD, requested a six-month delay, pushing back implementation to Jan. 1, 2021, "at the earliest."

London-based imaging tech company Behold.ai received the green-light for its red dot “instant triage” platform.

Current procedural terminology fixes helped stymie a concerning growth in the use of extremity nonvascular ultrasound, researchers reported in Current Problems in Diagnostic Radiology.

The House Ways & Means Committee unveiled its proposal earlier this month, which includes a mediation process that does not exclude providers based on an established qualifying threshold.