FAQs
What is Type I collagen?
Type I collagen is the most abundant structural protein in the human body. It provides mechanical strength and biological cues that regulate tissue healing. It is widely used in medical devices, wound care, and regenerative therapies.
Where does the collagen come from?
We source collagen from approved bovine or porcine tissues with strict control over traceability and quality. Only high-collagen-content tissues, such as tendons, are selected to ensure optimal bioactivity.
How is the collagen extracted?
Through a gentle enzymatic process, we separate collagen from other tissue components while preserving its triple-helix molecular structure. This structure is essential to its regenerative function.
Is the collagen purified?
Yes. After extraction, the collagen undergoes multiple purification steps—filtration, pH stabilization, and sterile processing—to achieve pharmaceutical-grade purity. All impurities, fats, and endotoxins are removed.
What are semi-finished collagen products?
Semi-finished forms of collagen include membranes, sponges, gels, and fibers. These intermediate materials are used to create finished medical devices or therapeutic products.
How are finished collagen medical devices made?
The semi-finished materials are shaped, crosslinked if needed, and sterilized under carefully controlled conditions. They are then packaged according to ISO and regulatory standards for clinical use.
Does your process preserve collagen’s regenerative potential?
Absolutely. We design every step of our process to maintain the collagen’s natural bioactivity. This ensures that the final product effectively stimulates cell migration, fibroblast activation, angiogenesis, and tissue repair.
Is your collagen CE- and FDA-compliant?
Yes. All of our finished products are manufactured to comply with the latest CE and FDA regulatory requirements, including rigorous testing for safety, efficacy, and biocompatibility.