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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October 4, 2018 in Dilumen, Lumendi, News, Press Release

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... Read More
August 21, 2018 in Lumendi, News, Press Release, Uncategorized

LUMENDI EXPANDS TEAM WITH NEW VP OF SALES, MICHAEL R. THOMAS

WESTPORT, CT, August 21, 2018 – Connecticut-based medical device innovator Lumendi, LLC is again expanding its team as Michael R. Thomas joins as Vice President of Sales. Mr. Thomas is... Read More
July 17, 2018 in Dilumen, Lumendi, News, Press Release

LUMENDI OPENS EU MARKET FOR DILUMEN EIP

CE Certification Confirms Device Conforms to Medical Device Directive 93/42/EEC BUCKINGHAMSHIRE, UK,  JULY 17, 2018 -- Lumendi Ltd., a privately held innovative medical device company, today announced that its subsidiary,... Read More