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Artiness’ ARTICOR planner receives FDA 510(k) clearance as a software to plan structural heart and vascular procedures

DateMarch 27, 2026
CategoriesCohort News
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Artiness has received FDA 510(k) clearance for ARTICOR Planner, its software for planning structural heart and vascular procedures. The clearance is a key step for the company’s mixed-reality technology and its mission to transform structural heart procedures, making ARTICOR Planner ready to enable advanced pre-operative planning based on patient-specific imaging in the U.S.

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