Calcium Hydroxylapatite Price
Ingredient: 26mg/ml HA, Hydroxyapatite 30%
Specification: 1ml
Package: Single package
Application Area: Brow bone, temple, nose shaping, apple muscle, decree line, puppet line, chin, etc.
Product Introduction:
The product contains a high concentration of sodium hyaluronate, allowing it to achieve a firm and natural effect immediately after injection. Additionally, the hydroxyapatite used in the formulation has highly porous microspheres, which provide a larger specific surface area for interactions with fibroblasts. This enhances protein and cell adhesion, increasing the likelihood of self-growth factor enrichment.
Product Display:
Product Details:
Type | |
Ingredient | Hyaluronic 26mg/ml, hydroxyapatite 30% |
Specification | 1ml |
Effect area | Subcutaneous injection |
Application area | Brow bone, temple, nose shaping, apple muscle, decree line, puppet line, chin, etc |
How to choose | Moderate to severe naso-lip wrinkles |
Package | Single package |
Storage | Cool, dry environment |
Recommended | 1-2 pc/time |
Recommended interval | 12-24 months |
Lasting time | 18-24 months |
Microsphere size | 25-45μm |
Extruding force | 23N (27G thin-walled needle) |
Product Package:
Customer Feedback:
Raw Material Advantages:
1. Sodium hyaluronate penetrates deep into the dermis, instantly revitalizing the skin and delivering an immediate firming and lifting effect. Hydroxyapatite stimulates collagen fiber production, effectively repairing the skin’s internal structure and supporting natural collagen regeneration. Over time, a dense and refined collagen network forms within the skin, ensuring a long-lasting lifting effect.
2. The FDA-approved Radiesse microcrystal filler is recognized as an ideal semi-solid, non-surgical facial filler. Currently, no “hydroxyapatite microsphere facial filler” products have been approved by the National Medical Products Administration (NMPA) in China.
Development Process:
Company Introduction:
The synthesis of PCL/PLLA on our platform is characterized by low tin content (Sn <30 ppm), controlled molecular weight, and compliance with medical-grade biocompatibility standards, utilizing custom-designed synthesis equipment that operates under anhydrous, oxygen-free conditions for kilogram-scale production. Moreover, our purification technology transforms industrial-grade raw materials into sterile, pyrogen-free medical-grade substances, such as sodium hyaluronate, carboxymethyl starch, and carboxymethyl cellulose.