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Medtech stories we missed this week: Dec. 22, 2017

December 22, 2017 By Danielle Kirsh

missed-medtech-0922From Hepa Wash’s new collaboration to Stimwave’s FDA clearance, here are five medtech stories we missed this week but thought were still worth mentioning.

1. Hepa Wash collaborates with GALS program

Hepa Wash announced in a Dec. 7 press release that it has collaborated with the German Accelerator Life Sciences (GALS) program to expand its company into the U.S. Hepa Wash recently introduced an Advanced Organ Support (ADVOS) procedure that offers multi-organ support for liver, lungs and kidneys while correcting acid-base balance disorders.

2. FDA clears Camber Spine interbody device

Camber Spine has received FDA 510(k) clearance for its Spira-C Open Matrix Cervical Interbody device, according to a Dec. 7 press release. The Spira-C Open Matrix Cervical Interbody is an interbody fusion implant that enhances fusion. It is the second implant clearance of the company and is a 3D printed titanium implant. It supplies the optimal environment for cell proliferation and bone growth.

3. NanoVibronix inks U.K. distribution deal

NanoVibronix announced in a Dec. 5 press release that it has entered a distribution agreement with BHR Pharmaceuticals to distribute its PainShield in the U.K. PainShield is an alternative to opioids for pain relief following surgery. It is an ultrasound-based product that is designed to treat pain in nerves, muscles, joints and soft tissue using localized ultrasound that heals soft tissue.

Get the full story on our sister site, MassDevice.

Filed Under: Diagnostics, Featured, Food & Drug Administration (FDA), Hospital Care, Imaging, Implants, Pain Management, Regulatory/Compliance, Surgical Tagged With: Camber Spine, Hepa Wash, In2Bones, medtech, NanoVibronix, Stimwave

IN CASE YOU MISSED IT

  • Medtronic moves to divest final stake in MiniMed
  • 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 

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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