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510(k) submission for ProgenaMatrixFLEX™ is under review by the FDA

Cell Constructs submitted the 510(k) premarket notification for ProgenaMatrixFLEX™, our next generation Human Keratin Matrix. The submission is currently under review by the FDA.

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ProgenaMatrix™ is a medical device cleared by the US FDA for the treatment of dry and exuding partial and full thickness wounds.

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