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Medtech stories we missed this week: Dec. 8, 2017

December 8, 2017 By Danielle Kirsh

medtech missed
[Image from unsplash.com]
From Minimus Spine’s European distribution deal to Stimwave receiving FDA clearance, here are seven medtech stories we missed this week but thought were still worth mentioning.

1. Minimus Spine inks EU distribution deal

Minimus Spine announced in a Dec. 4 press release that it has signed its first European distribution deal with Italian company Moss and has completed its first commercial order. Moss has exclusive distribution rights to distribute in Italy, Germany, Switzerland and the U.K.

2. Elanix, Dermacon sign wound management development deal

Elanix Biotechnologies and Dermacon have signed an agreement to develop progenitor cell medical devices that help accelerate wound healing, according to a Dec. 1 press release. The new devices, called First Cover, will use Elanix’s progenitor cell technology and will be evaluated to accelerate healing in acute and chronic wounds. Dermacon will design progenitor cell matrix-based products for Elanix and guide the development and CE mark processes.

3. CSA Medical launches TruFreeze Rapid AV trial

CSA Medical announced in a Nov. 27 press release that it has enrolled its first patient into a multi-center prospective study that determines the effects of spray cryotherapy on patients who have esophageal cancer. The patient received treatment at the University of North Carolina’s Center for Esophageal Diseases and Swallowing.

Get the full story on our sister site, MassDevice.

Filed Under: Business/Financial News, Cardiovascular, Diagnostics, Featured, Food & Drug Administration (FDA), Oncology, Pain Management, Regulatory/Compliance, Surgical, Technology Tagged With: Cagent Vascular, CSA Medical, Dermacon, Elanix, InspireMD, Life Spine Inc., medtech, Minimus Spine, Stimwave

IN CASE YOU MISSED IT

  • Dexcom adds former Stryker CFO to board
  • MiniMed wins CE mark for next-gen insulin pump, ups revenue guidance
  • Abbott wins FDA authorization for dual glucose-ketone sensor
  • FDA clears Roche’s Alzheimer’s blood test for rule-in and rule-out assessment 
  • MiniMed Flex now integrated with Abbot’s Instinct sensor 

About Danielle Kirsh

Danielle Kirsh is an award-winning journalist and senior editor for Medical Design & Outsourcing, MassDevice, and Medical Tubing + Extrusion, and the founder of Women in Medtech and lead editor for Big 100. She received her bachelor's degree in broadcast journalism and mass communication from Norfolk State University and is pursuing her master's in global strategic communications at the University of Florida. You can connect with her on Twitter and LinkedIn, or email her at [email protected].

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