Omeza Receives FDA Clearance for Omeza® Collagen Matrix
Business
SRQ DAILY MONDAY BUSINESS EDITION
MONDAY SEP 6, 2021 |
Omeza, a Sarasota-based skin science company, announced recently the U.S. Food and Drug Administration (FDA) cleared Omeza® Collagen Matrix through the FDA 510(k) premarket notification process. Omeza® Collagen Matrix is Omeza’s first Rx product, and the first drug/device combination matrix of its kind for chronic wound care.
“No one is taking on the challenge of making advanced wound care products both effective and affordable, yet preventable amputations are on the rise. We are determined to bridge that gap,” said Sarah Kitlowski, President of Omeza. “Our mission is to give practitioners groundbreaking new tools to help protect and manage the wound during the natural processes of wound closure.”
Omeza® Collagen Matrix (OCM) is a wound care matrix comprised of hydrolyzed fish collagen infused with cod liver oil, which acts as an anhydrous skin protectant, and other plant-derived oils and waxes. When applied to a wound surface, the matrix is naturally incorporated into the wound over time. Omeza® Collagen Matrix is designed for intimate contact with both regular and irregular wound beds to provide a conducive environment for the patient’s natural wound healing process. The product features a no-prep application supplied in easy-to-use, unit dose vials.
Inquiries from medical and health professionals should be directed to info@omezapro.com.
Image courtesy of Omeza
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