August 20, 2019 in Dilumen, EIP, Lumendi, Press Release, Uncategorized

LUMENDI RECEIVES 510(k) CLEARANCE FOR DILUMEN Ik™ ENDOLUMENAL INTERVENTIONAL KNIFE

1000 Therapeutic Procedures Using DiLumen™ EIP Completed Across U.S., Europe and Asia   WESTPORT, CONN, August 20, 2019 − Connecticut-based medical device innovator Lumendi, LLC (http://www.lumendi.com) has announced it has received... Read More
June 11, 2019 in Dilumen, EIP, Lumendi, Press Release, Uncategorized

LUMENDI BRANDS EXCLUSIVE TISSUE MANIPULATION FEATURE FOR COMPANY’S DILUMEN EIP

DiLumen +DR Dynamic Retraction System Improves Endoscopists’ Ability to Dissect and Ultimately Resect Polyps Without Surgical Intervention WESTPORT, CONN, June 11, 2019 — Connecticut-based medical device innovator Lumendi, LLC has launched... Read More
June 10, 2019 in Lumendi, News, Press Release, Uncategorized

LUMENDI RECEIVES FDA 510(k) CLEARANCE FOR DILUMEN C2TM

Second Generation Endoscopic Accessory for Endolumenal Procedures WESTPORT, CONN, April 23, 2018 – Connecticut-based medical device innovator Lumendi, LLC has announced it has received United States Food and Drug Administration... Read More
November 13, 2018 in Dilumen, Lumendi, News, Press Release

LUMENDI RECEIVES FDA 510(k) CLEARANCE FOR INNOVATIVE DILUMEN EIP DEVICE MODIFICATION TO IMPROVE TISSUE RETRACTION DURING THERAPEUTIC ENDOSCOPY

With recent regulatory approvals in Europe, Lumendi has established distribution in the UK, France and Italy and has conducted successful procedures with clinicians in each country.

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