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April 25th marks the beginning of the 2018 Symposium for Advanced Wound Care, and the Wound Healing Foundation (WHF) will be in attendance. While at the Symposium, the WHF will present three major awards, as well as a dozen recognition and travel awards and facilitate two lectures. For those that wish to attend, the schedule is as follows.

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Christchurch, New Zealand – March 28, 2018 – Two new smart-phone based imaging products, SilhouetteLite+ and SilhouetteLite, recently launched by ARANZ Medical Limited have been adopted by Promore Pharma AB (Solna, Sweden) for a multi-site clinical trial, and by New Zealand's Capital and Coast District Health Board for their community-based nurses.

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By the WoundSource Editors

Foundation News

The Wound Healing Foundation (WHF) was selected as a potential recipient in the 2017 Combined Federal Campaign (CFC ). The CFC program allows federal employees to donate to selected charities. Encourage all federal employees and military personnel to donate to the WHF and use our CFC #88674.

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Schertz, TX – March 13, 2018 – EZ Debride®, a registered and patent pending brand of MDM Wound Ventures LLC, developed and manufactured out of Schertz, Texas and Millersburg, Pennsylvania, is announcing the distribution agreement with BMK Ventures, Virginia Beach, Virginia.

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Pennington, NJ – March, 7 2018 – Dermalink Technologies Inc. (Dermalink) is pleased to announce the development of the first of its novel biofilm-disrupting products for the U.S. wound care market. The core ingredient, Lauroyl Arginine Ethylester (LAE), has been available in Europe for several years, where it has rapidly established itself as a proven anti-biofilm agent in the food and dental markets.

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In their quarterly Alliance Advocacy Update, the Alliance of Wound Care Stakeholders (Alliance) provides a review of 2017, and looks ahead to their plans and goals 2018.

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By the WoundSource Editor

Newport Beach, CA – January 9, 2018 –Ventris Medical, a Newport Beach-based healthcare company, today announced the company’s official launch. The company also is launching its full line of placental allograft products that will be used in surgical and non-surgical applications.

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By the WoundSource Editors

Suwanee, GA – January 2, 2018 – SANUWAVE Health, Inc. (OTCQB: SNWV) has announced that the US Food and Drug Administration (FDA) has issued its decision on the de novo submission for the dermaPACE® System. Their decision, dated December 28, 2017, permits the marketing of the dermaPACE System as a Class II medical device used for the treatment of Diabetic Foot Ulcers (DFU) in the U.S., the world's largest medical device market. This order by FDA is the culmination of intensive clinical studies by SANUWAVE and diligent work by both SANUWAVE employees and their regulatory partners, Musculoskeletal Clinical Regulatory Advisers (MCRA) in successfully submitting documentation and interacting with FDA during the clearance process.

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By the WoundSource Editor

Tempe, Arizona - December 5, 2017 Vomaris Innovations, Inc. announced today breakthrough results of the first controlled, preclinical in vivo evidence on the anti-biofilm impact of the company’s bioelectric antimicrobial technology. The study found that the technology can prevent and disrupt biofilm infection and restore functional wound healing. The manuscript, “Electric Field Based Dressing Disrupts Mixed-Species Bacterial Biofilm Infection and Restores Functional Wound Healing,” was published online in the Annals of Surgery. The research was led by Chandan Sen, Ph.D., Professor of Surgery and Director of the Comprehensive Wound Center at The Ohio State University’s Wexner Medical Center.

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by The Wound Healing Foundation

This update from the Wound Healing Foundation (WHF) provides an overview of current and future educational, research and community-based initiatives in wound care. Recent WHF activities and opportunities include participation in international dialogue and meetings, as well as the ongoing efforts to advance and support scientific research in the field of wound management.

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