Global Pathways to Aesthetic Innovation

Leverage our portfolio of 20+ Class III medical devices, including NMPA-approved innovations and CE-pending technologies, to build your competitive edge through flexible collaboration frameworks in your local area.

Joint Registration

Co-develop and co-regulate products in target markets. 
We provide technology and pre-clinical/clinical data;
Our partner contributes local regulatory expertise and resources.
We Thrive with Partners Who have:
Proven success in international medical device approvals

Proven success in international medical device approvals

Capabilities to support region-adapted clinical validation

Capabilities to support region-adapted clinical validation

Cross-border regulatory network resources

Cross-border regulatory network resources

Platform Technology Transfer

Acquire complete biomaterial platforms (e.g., polymer microspheres, dECM) for autonomous product development.
Flexible collaboration frameworks in your local area.
We Thrive with Partners Who have:

Exclusive Regional Distribution

Obtain exclusive rights to market approved products in your territory. 
We handle manufacturing and shipment to partner’s warehouse 
Our partner manages sales channels and local market penetration.
We Thrive with Partners Who have:
Remarkable market presence in aesthetic/medical distribution

Remarkable market presence in aesthetic/medical distribution

Capabilities to support region-adapted clinical validation

Capabilities to support region-adapted clinical validation

Cross-border regulatory network resources

Cross-border regulatory network resources

New-co Venture

Co-establish a new entity for targeted markets/products.
We contribute IP tech;
Our partner provides capital commercialization infrastructure;
Equity-based collaboration.
We Thrive with Partners Who have:

Togehter, let’s architect your global aesthetics leadership strategy.

July.06.2023
The parties have entered into a 10-year exclusive master distribution agreement covering two advanced aesthetic products: the Sodium Hyaluronate Injectable Complex Solution and a new-generation Injectable PLLA Microsphere Facial Filler.
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July.10.2025
The injectable poly-L-lactic acid (PLLA) microsphere filler is classified as a Class III medical device and is currently undergoing registrational clinical trials in China. The product utilizes a patented microsphere fabrication process, resulting in uniformly shaped microspheres with even subcutaneous distribution and outstanding clinical performance.
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March.29.2025
Xihong Biopharma showcased its regenerative medicine solutions—combining advanced science, innovative manufacturing, and global partnerships. As a leading innovator from China, Xihong impressed attendees with its deep expertise and comprehensive portfolio in regenerative aesthetics.
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