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Lumendi secured 510(k) clearance from the FDA for its endoscopic accessory called DiLumen C2, which is designed to ensure tha -More-
European regulators have granted Lumendi approval for its single-use DiLumen Endolumenal Interventional Platform device, whic -More-
Medical devices maker Lumendi has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its DiLumen Is endolumenal interventional scissors.
Lumendi's DiLumen Is endolumenal interventional scissors were granted 510(k) clearance by the FDA. -More-
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 an accomplished medical/su...
CE Certification Confirms Device Conforms to Medical Device Directive 93/42/EEC Lumendi Ltd., a privately held innovative medical device company, today announced that i...
Second Generation Endoscopic Accessory for Endolumenal Procedures Connecticut-based medical device innovator Lumendi, LLC (http://www.lumendi.com) has announced it has receive...
Connecticut-based medical device innovator Lumendi, LLC (http://www.lumendi.com) reports that more than 500 therapeutic procedures by more than 40 endoscopists and colorectal surg...
http://www.lumendi.com Lumendi, Ltd., is a privately held innovative, medical device company headquartered in Buckinghamshire, UK. Lumendi is focused on developing, marketi...
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