1. Lumendi Receives FDA 510(k) Clearance For Innovative DiLumen EIP Device Modification – Health Device Network

    Lumendi Receives FDA 510(k) Clearance For Innovative DiLumen EIP Device Modification – Health Device Network

    Medical device innovator Lumendi LLC has received U.S. Food and Drug Administration (FDA) clearance for its DiLumen EIP technology with ‘suture loops’ placed in the skirt along the trailing edge of the fore balloon. This new device feature will help facilitate tissue manipulation for easier dissection and resection of polyps without the need for surgical intervention. 

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