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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,...

FLEXIBLE ENDOSCOPIC DOUBLE BALLOON PLATFORM: FROM CONCEPT TO HUMAN FEASIBILITY TRIAL

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Flexible Endoscopic Double Balloon Platform: from concept to human feasibility trial. Sam Sharma*, Kota Momose, Toyooki Sonoda, Reem Z. Sharaiha Weill Cornell Medical College, New York, NY Background: Despite the...

LUMENDI RECEIVES FDA 510(k) CLEARANCE FOR DILUMEN Is ENDOLUMENAL INTERVENTIONAL SCISSORS

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Second Generation Endoscopic Accessory for Endolumenal Procedures WESTPORT, CONN, May 29, 2018 − Connecticut-based medical device innovator Lumendi, LLC has announced it has received United States Food and Drug Administration...

LUMENDI RECEIVES FDA 510(k) CLEARANCE FOR DILUMEN C2™

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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...