CapsoVision, a medical device company, submitted a 510(k) application to the FDA for an AI-assisted module designed for its CapsoCam Plus capsule endoscopy platform. The tool aims to improve ...
(NASDAQ: CV), a commercial-stage medical technology company developing advanced imaging and AI-enabled capsule endoscopy solutions, today announced submission of its 510(k) application to the Food and ...
StimLabs announces that the U.S. Food & Drug Administration (FDA) has granted 510 (k) clearance for Theracor, the first human umbilical cord-derived medical device to be offered in sheet form. This ...
Next-Generation Novasight Hybrid System Submitted to U.S. FDA for 510(k) Clearance U.S. and European Class 1A Guidelines Reinforce Growing Adoption of Image-Guided PCIPeer-Reviewed Publications Highli ...
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Conavi Medical advances hybrid intravascular imaging platform as revenue jumps in fiscal 2025
An update from Conavi Medical ( ($TSE:CNVI) ) is now available. Conavi Medical reported that fiscal 2025 marked a pivotal year, highlighted by the ...
Next-Generation Novasight Hybrid™ System Submitted to U.S. FDA for 510(k) Clearance U.S. and European Class 1A Guidelines Reinforce Growing ...
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