Lumendi news

The latest news about Lumendi

LUMENDI REPORTS SUCCESSFUL ENROLLMENT CLOSURE OF ITS DILUMEN™ ENDOLUMENAL INTERVENTIONAL PLATFORM (EIP™) STUDY

The study evaluates DiLumen’s effect on endoscopic procedure time for pre-cancerous colorectal complex polypectomies.

LARGE COMPLEX POLYPS REMOVED SUCCESSFULLY FROM THREE PATIENTS WITHOUT SURGICAL INTERVENTION USING LUMENDI DILUMEN C2™

The first successful case at Cleveland Clinic using DiLumen C2 was completed by Dr. Gorgun when a large complex polyp in the distal sigmoid, 18cm from the anus was removed from a 72-year-old woman with a narrow sigmoid.

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 U.S.… Continue reading LUMENDI RECEIVES 510(k) CLEARANCE FOR DILUMEN Ik™ ENDOLUMENAL INTERVENTIONAL KNIFE

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

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… Continue reading LUMENDI RECEIVES FDA 510(k) CLEARANCE FOR DILUMEN C2TM

MEDICAL MARVELS with Eyewitness News

MEDICAL MARVELS   Dual balloon endoscope device reduces the need for surgery to remove polyps.   As seen on Eyewitness News | Tuesday, January 29, 2019 12:00AM UPPER EAST SIDE, Manhattan… Continue reading MEDICAL MARVELS with Eyewitness News

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.

500 THERAPEUTIC PROCEDURES USING DILUMEN EIP COMPLETED ACROSS U.S., EUROPE AND ASIA

WESTPORT, CONN, OCTOBER 4, 2018 − Connecticut-based medical device innovator Lumendi, LLC reports that more than 500 therapeutic procedures by more than 40 endoscopists and colorectal surgeons have been completed… Continue reading 500 THERAPEUTIC PROCEDURES USING DILUMEN EIP COMPLETED ACROSS U.S., EUROPE AND ASIA