About Xihong Biopharma

Your Open Innovation Partner in Regenerative Medicine

XIHONG BIOPHARMA

10+ Years

Deep domain expertise in biomaterials

20+ Products

Class III injectables

60+ Patents

Core IP in polymer microspheres
Established in 2016, we pioneer end-to-end solutions for regenerative medicine medical devices.

From R D to commercial scale manufacturing. Through open collaboration models including ODM, CDMO, technology transfer, and joint ventures ("new-co").

Technology Breakthroughs & Commercialization

—Powering Aesthetic Innovation
Through oxygen-free vacuum polymerization, we achieve 99.8% monomer conversion – the industry’s highest yield – ensuring batch-to-batch consistency at kilogram-scale production. Advanced directional modification technology creates bespoke PLLA/PCL composites with tunable hydrophilicity, antimicrobial properties, and collagen-stimulating capabilities.
We overcome critical limitations in regenerative biomaterials with CRISPR-edited, zero-immunogenicity ECM. Our enzymatic decellularization process preserves 95% of native collagen/elastin structures while eliminating immune risks.
As pioneers in microfluidic manufacturing (China’s first operational line), we produce perfectly uniform microspheres (30-80μm ±0.6 dispersity) at 90% yield – 4.5× industry average

Production & Capacity

—Scalable, Flexible Manufacturing Engineered for Partnership
Compliant infrastructure aligned with China NMPA and EU MDR/FDA standards.
Home to China s first microfluidic production line.
5 dedicated workshops housing 9 advanced production lines. Our 33,000㎡ flagship facility delivers 10M+ annual doses — the largest biomaterials output in China.

Partner with Us

—From Lab to Global Markets

Together, we transform science into globally compliant, high-impact products.
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Channel leaders

Channel leaders

Distributors, aesthetic chains...
Market-ready innovators

Market-ready innovators

Biotechs, medtech firms
Strategic investors

Strategic investors

Seeking turnkey regenerative medicine portfolios

We empower partners with:

  • 20+ Class III injectables in pipeline – Licensable technologies

  • Global Pathways: NMPA registration (2025 China launch) → CE Marking (EU entry prep)

  • Flexible commercialization pathways to accelerate product value realization.

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