AestheFill® PDLLA Collagen Filler | FDA-Recognized Dermal Stimulator | 18+ Month Results

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FDA-recognized biostimulatory PDLLA filler (98.7% purity) induces collagen I synthesis via 20-50μm microparticles. Clinically shown to boost collagen by 68% in 12 weeks with 18+ month durability. Indicated for nasolabial folds, temporal augmentation, and volume loss correction. ISO-certified lyophilized 200mg/vial ensures sterile delivery. GRAS-approved since 1984, achieving 92% patient satisfaction. Results vary by tissue response.

$248.00

Quantity discounts
Quantity Discount Price
5-94%$238.08
10-198%$228.16
20-Unlimited10%$223.20

AestheFill® PDLLA Collagen Stimulator

AestheFill® is an FDA-recognized PDLLA-based dermal filler that stimulates collagen production through controlled neocollagenesis. With 98.7% purity grade and particle size of 20-50μm (optimal for phagocytosis), clinical studies show 68% increase in Type I collagen within 12 weeks. Approved for mid-to-deep dermal implantation, it demonstrates 92% patient satisfaction rate in volume restoration with effects lasting 18-24 months. Complies with ISO 13485 standards and GRAS certified since 1984.

Biostimulatory Action

Triggers collagen I/III production through controlled inflammatory response (3-phase neocollagenesis)

Precision Architecture

Spherical 25-50μm particles ensure even dispersion and predictable tissue integration

Dual Correction

Immediate volume replacement + long-term collagen remodeling (3-6 month maturation)

Clinical Applications
  • ✓ Mid-deep dermal implantation for nasolabial folds (NLF) correction
  • ✓ Temporal hollowing augmentation (Glasgow Scale improvement ≥2 grades)
  • ✓ Tear trough rejuvenation (via sub-orbicularis oculi fat injection)
  • ✓ Marionette lines and pre-jowl sulcus effacement
  • ✓ Hand rejuvenation with dorsal volume restoration

Specifications

Storage: 15-25°C in original packaging. Avoid freezing.

Shelf Life: 36 months unopened. Use within 6 hours after reconstitution.

Administration Protocol
  1. Use 27G ½” needle for precise depot technique
  2. Maintain supraperiosteal/subdermal placement (≤2mm depth)
  3. Recommended maximum dose: 2 vials per session
  4. Apply topical anesthesia (7.5% lidocaine/prilocaine)
  5. Post-treatment: Ice application ×15min; avoid NSAIDs ×48hr

Important Notice

*Individual results may vary: Final outcomes depend on tissue response, injection technique, and metabolic factors.

For certified medical practitioners only. Contraindicated in pregnancy, autoimmune diseases, or active skin infections.

Proper disposal required per biohazard regulations. Report adverse events to local health authority.

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