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FDA Clears First-in-World Hematology App, Unlocking Potential of Diagnosis

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Scopio Labs, a leading provider of Full Field Morphology (FFM), announced that it was granted FDA clearance to market and sell its X100 with Full Field Peripheral Blood Smear (Full Field PBS) Application, unlocking the potential of in vitro hematology diagnosis. Full Field PBS is also available in Europe with CE mark certification granted earlier this year. Blood is one of the most foundational gateways to health information. Even with the adoption of digital tools, today's solutions do not showcase all required regions of interest in a PBS slide, only capturing snapshots of cells. To help improve diagnostic accuracy leveraging novel computer vision tools, Full Field PBS gives clinical laboratories an unprecedented ability to capture digital scans using advanced computational photography imaging and tailored AI tools.


Aidoc's 6th FDA clearance for AI Solution

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Aidoc announced today that the US Food and Drug Administration (FDA) has given regulatory clearance for the commercial use of its triaging and notification algorithms for flagging and communicating incidental pulmonary embolism . Flagging incidental, critical findings is a huge technical challenge due to the varied imaging protocols used and lower incidences of such cases. The ability to prioritize incidental critical conditions accurately is a breakthrough in the value AI can bring to the radiologist workflow. "The most common use case we experienced is for critical unsuspected findings in oncology surveillance patients" said Dr. Cindy Kallman, Chief, Section of CT at Cedars-Sinai Medical Center. "The ability to call the referring physician while the patient is still in the house is huge. We are essentially offering a point-of-care diagnosis of PE for our outpatients. Our referring physicians have been completely wowed by this."


Israel's Zebra Medical Gets FDA Clearance for Mammography Tool

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Zebra Medical Vision, an Israeli medical imaging analytics company, said on Monday it received clearance from the U.S. Food and Drug Administration for its mammography technology. The company's latest cleared product uses artificial intelligence to prioritize and identify suspicious mammograms. The mammograms are automatically sent to Zebra's platform, where they are processed and analysed for suspected breast lesions. The HealthMammo product then returns its result to the radiologist. It is the company's first oncology tool to receive FDA clearance.


FDA clearance gives wings to Indian AI tool for fast diagnosis

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Mumbai-based startup Qure uses an AI imaging tool qER to save precious minutes for emergency room staff to take action based on head CT scans. After deployment in India and several other countries, qER is now entering the US where 75 million CT scans are performed every year. A couple of weeks ago, Qure received US FDA 510 (k) clearance for this product. What makes it special is a four-in-one clearance. The tool has been cleared for triaging four critical conditions--intracranial bleeds, mass effect (due to spaces in the brain filling up), midline shift (in the brain's alignment), and cranial fractures.


AI that flags urgent cases for radiologists gets FDA clearance - MedCity News

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Nines, a Palo Alto-based teleradiology startup, received FDA 510(k) clearance for a system that can detect and triage two serious conditions from CT scans. The company's NinesAI system uses machine learning to identify potential cases of intercranial hemorrhage and mass effect, both of which are associated with strokes. The system then flags those cases for expedited review by radiologists. For both of these conditions, every hour counts toward a patient's survival. "This has been a long time coming. A lot of hard work went into it," CEO David Stavens said in a phone interview.


Aidoc expands sales team after gaining FDA clearance for AI system

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Aidoc, a Tel-Aviv, Israel-based medical imaging company, announced back in August that it had gained FDA clearance for a new solution that helps radiologists triage patients using artificial intelligence (AI). Now, to meet an increase in customer demand as a result of that announcement, the company has hired Tom Shearer to manage sales in North America and Jeremy De Sy to handle sales throughout Europe. "AI isn't the future for medical imaging; it's the present," Shearer said in a prepared statement. "Aidoc is led by extraordinary individuals who have developed a revolutionary product. This solution is always running in the background, on every exam, filling a critical need in medical imaging by helping radiologists manage their increasing workload while maintaining high standards."