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https://www.prnewswire.com/news-releases/geneditbio-receives-fda-clearance-of-ind-application-for-its-lead-in-vivo-genome-editing-program-geb-101-for-tgfbi-corneal-dystrophy-302652666.html GenEditBio Receives FDA Clearance of IND Application for Its Lead In Vivo Genome-Editing Program... receives fda clearance ind lead https://info.pathai.com/pathai-receives-fda-clearance-for-aisight-dx PathAI’s AISight® Dx Receives FDA Clearance for Use in Primary Diagnosis Sep 9, 2025 - PathAI has received 510(k) clearance from the FDA for AISight® Dx—PathAI’s digital pathology image management system—for use in primary diagnosis in... dx receives fda clearance use https://www.pathai.com/aisightdx-digital-pathology-solution PathAI’s AISight® Dx Receives FDA Clearance for Use in Primary Diagnosis Sep 9, 2025 - PathAI has received 510(k) clearance from the FDA for AISight® Dx—PathAI’s digital pathology image management system for use in primary diagnosis in... dx receives fda clearance use https://www.prnewswire.com/news-releases/abbotts-amplatzer-piccolo-delivery-system-receives-fda-clearance-and-ce-mark-to-optimize-procedures-for-premature-babies-with-a-hole-in-the-heart-302645632.html Abbott's Amplatzer Piccolo™ Delivery System Receives FDA Clearance and CE Mark to Optimize... /PRNewswire/ -- Abbott (NYSE: ABT) today announced it has received U.S. Food and Drug Administration (FDA) clearance and CE Mark for its Amplatzer Piccolo™... receives fda clearance abbott https://neuronewsinternational.com/methinks-ai-receives-us-fda-510k-clearance-for-ncct-stroke-software/ Methinks AI receives US FDA 510(k) clearance for NCCT Stroke software Jul 1, 2025 - Methinks AI announced today that its non-contrast computed tomography (NCCT) Stroke software has received 510(k) clearance from the US Food and Drug... k clearance methinks ai receives https://www.prnewswire.com/news-releases/aqualung-therapeutics-receives-fda-clearance-for-phase-2a-lung-fibrosis-study-302648010.html Aqualung Therapeutics Receives FDA Clearance for Phase 2a Lung Fibrosis Study /PRNewswire/ -- Aqualung Therapeutics, a clinical-stage immunotherapeutics company, announced today that the Food and Drug Administration (FDA) has cleared... therapeutics receives fda lung https://www.femtechworld.co.uk/news/smart-baby-monitoring-device-receives-fda-clearance/ Smart baby monitoring device receives FDA clearance - FemTech World Jun 22, 2023 - The device provides a real-time display of the baby’s heart rate and oxygen saturation level receives fda clearance smart