EYSINS, Switzerland, April 3, 2025 /PRNewswire/ --Today, AliveDx announces it has submitted 510(k) premarket notification to the U.S. Food and Drug Administration (FDA) for the MosaiQ AiPlex ...

Proprio, the global leader in AI-powered surgical technology, announced that its AI guidance platform for surgery, Paradigm, has received its second major 510(k) clearance from the US Food and Drug ...

Pixee Medical, a pioneer in Augmented Reality (AR) navigation for orthopedic surgery, announces FDA 510(k) clearance of Knee+ NexSight, the cutting-edge AR guidance solution for total knee ...

Morningstar brands and products Company Portfolio ...

(RTTNews) - Daxor Corporation (DXR), Thursday announced the submission of its next-generation blood volume analyzer - Daxor BVA - to the Food and Drug Administration (FDA). The company says that ...

BESANÇON, France--(BUSINESS WIRE)--Pixee Medical, a pioneer in Augmented Reality (AR) navigation for orthopedic surgery, announces FDA 510(k) clearance of Knee + NexSight, the cutting-edge AR guidance ...

AliveDx CEO Manuel Méndez said in a statement that the FDA 510(k) submission brings the company closer to delivering clinical and economic value to its US customers. "With autoimmune disease diagnoses ...

EYSINS, Switzerland, April 3, 2025 /PRNewswire/ --Today, AliveDx announces it has submitted 510(k) premarket notification to the U.S. Food and Drug Administration (FDA) for the MosaiQ AiPlex ® ...