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Medtech stories we missed this week: April 27, 2018

April 27, 2018 By Danielle Kirsh

canyon at sunset
[Image from unsplash.com]
From DuPuy Synthes’s spinal implant launch to Lumendi’s FDA clearance, here are seven medtech stories we missed this week but thought were still worth mentioning.

1. DePuy Synthes launches spinal implants

DePuy Synthes announced in an April 26 press release that it has launched its Proti 360º integrated titanium family of interbody devices that are designed to be used with patients who have degenerative disc disease in their neck and back. The Proti 360º is designed to maximize the potential for bone growth while offering the benefits of PEEK and titanium. Titanium creates a bioactive surface that promotes attachment and bone-forming cell growth.

2. PavMed to commercialize EsoCheck Barrett’s Esopagus biomarker test

PavMed has signed a letter of intent with Case Western Reserve University to commercialize its EsoCheck technology, according to an April 24 press release. EsoCheck is a non-invasive, cell-sampling device that features highly accurate DNA biomarkers that detect Barrett’s Esophagus. The device is offered as an office-based test that takes five minutes to complete. A patient swallows a vitamin pill-sized capsule that has a small inflatable balloon attached to a thin catheter. The balloon swabs the target area for cells as the catheter is removed. Then the sample can be tested for DNA biomarkers.

3. Cerus wins Health Canada nod for Intercept blood system

Cerus announced in an April 25 press release that it has won Health Canada approval to commercialize its Intercept Blood System for platelets. The system is designed for ex vivo treatment and storage of platelet components. It is used to inactivate a broad range of pathogens like viruses, bacteria and protozoan parasites to reduce the risk of transfusion-transmitted infections.

Get the full story on our sister site, MassDevice.

Filed Under: Featured, Food & Drug Administration (FDA), Hematology, Hospital Care, Orthopedics, Regulatory/Compliance Tagged With: abbott, apolloendosurgery, Cerus Corp., DePuy Synthes, lumendi, PAVmed, reshapelifesciences, sanquin

IN CASE YOU MISSED IT

  • Glooko adds chief strategy officer to chief medical officer’s title
  • Cordis launches 10,000-patient registry for drug-eluting balloon
  • Senseonics opens $50M public offering, $25M private placement with Abbott
  • Study links Abbott CGM use to lower risk of hospitalizations due to heart complications
  • Go-Pen ApS wins FDA nod for user-filled insulin pen

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 dkirsh@wtwhmedia.com.

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