Reno, Nevada– Conexeu Sciences Inc. (the “Company” or “Conexeu”) a biotechnology company revolutionizing tissue regeneration, is pleased to announce the completion of its $5 million Regulation Crowdfunding (Reg CF) financing. Conexeu secured commitments in excess of $5 million in less than two weeks from the date of launching the financing through the Equifund platform.

Conexeu Chief Executive Officer, Jeff Sharpe, stated, “This milestone highlights the strong investor confidence in Conexeu’s patented collagen platform and its potential to disrupt multi-billion-dollar markets in wound care, medical aesthetics, and tissue engineering.

Sharpe continued, “My team and I are grateful to both our investors and to Equifund for providing a funding platform that allowed us to connect with passionate supporters who share our vision for the future of regenerative medicine.”

Equifund Chief Executive Officer, Jordan Gillissie, said, “Conexeu’s successful funding demonstrates the power of the crowd to support groundbreaking technologies with the potential to change lives.”

The funds raised will be used to accelerate the development and commercialization of Conexeu’s patented collagen platform, which has the potential for broad applications across multiple verticals.  The Company is currently focused in five markets; wound care, veterinary medicine, 3D bioprinting, dental soft tissue repair, and medical aesthetics.

Regulation CF is regulated by the U.S. Securities and Exchange Commission. It allows companies to raise up to $5 million in a 12-month period from both accredited and non-accredited investors. Conexeu’s success in utilizing this funding regulation underscores the growing interest in crowdfunding as a viable and efficient way to fund innovative ventures.

Read Original Release: https://www.newsfilecorp.com/release/270602/Conexeu-Sciences-Closes-Maximum-5M-Reg-CF-Financing

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IMPORTANT NOTICES: CXU™ is a medical device candidate in preclinical development. It has not been submitted to or reviewed by the U.S. Food and Drug Administration. Safety and effectiveness have not been established. See Forward-Looking Cautionary Statement.Terms such as 'next-generation,' 'advanced,' 'innovative,' and 'bioregenerative' reflect the Company's assessment of its technology relative to existing approaches and are not intended as representations of regulatory status, clinical performance, or guaranteed commercial outcomes. CXU™ is an investigational medical device candidate. Safety and effectiveness have not been established. See Forward-Looking Cautionary Statement.