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

| Dilumen, Lumendi, News, Press Release | No Comments

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

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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...

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

| Lumendi, News, Press Release, Uncategorized | No Comments
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...

LUMENDI OPENS EU MARKET FOR DILUMEN EIP

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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,...