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

$256.00

AestheFill® PDLLA Collagen Filler is an FDA-recognized biostimulator delivering 98.7% pure PDLLA microparticles (20-50μm) for optimized collagen induction. Clinically proven to increase Type I collagen by 68% within 12 weeks with results lasting 18+ months.

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Description

AestheFill® PDLLA Collagen Filler

FDA-Recognized Dermal Stimulator | 18+ Month Results

Clinical-Grade Collagen Stimulation

FDA-recognized biostimulatory PDLLA dermal filler (98.7% purity) with 20-50μm microparticles optimized for phagocytosis. Clinically proven to increase Type I collagen by 68% within 12 weeks with durable results lasting 18+ months. ISO-certified lyophilized formulation provides sterile delivery, achieving 92% patient satisfaction in volume restoration therapies.

Key Clinical Advantages

Biostimulatory Action

Triggers collagen I/III synthesis through controlled inflammatory response

Precision Architecture

Spherical 20-50μm particles ensure even dispersion and predictable integration

Dual Correction

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

Longevity

18+ month durability proven in clinical evaluations

Technical Specifications

  • Material: Poly-D,L-lactic acid (PDLLA)
  • Purity: 98.7% pharmaceutical grade
  • Particle Size: 20-50μm optimized spheres
  • Certification: ISO 13485 & GRAS since 1984

Packaging Specifications

  • Form: Lyophilized powder
  • Content: 200mg/vial
  • Storage: 15-25°C in original packaging
  • Shelf Life: 36 months unopened

Clinical Applications

✓ Nasolabial folds correction ✓ Temporal hollowing augmentation (Glasgow Scale improvement ≥2 grades)
✓ Tear trough rejuvenation ✓ Marionette lines ✓ Pre-jowl sulcus effacement ✓ Hand rejuvenation

Professional Administration Protocol

Preparation

• Use within 6hr after reconstitution
• Apply 7.5% lidocaine/prilocaine anesthesia

Technique

• 27G ½” needle required
• Supraperiosteal/subdermal placement (≤2mm depth)
• Depot injection method

Dosage

• Max 2 vials per session
• Nasolabial folds: 0.8-1.2mL/side
• Temples: 1.0-1.5mL/side

Post-Treatment Care

Immediate: Ice application ×15min

Medication: Avoid NSAIDs ×48hr

Activity: Avoid strenuous exercise ×24hr

Follow-up: Assess at 4-week intervals

Medical Practitioner Notice

*Results vary based on tissue response and technique. For certified medical use only. Contraindicated in pregnancy, autoimmune disorders, or active infections. GRAS-certified since 1984. Report adverse events per FDA regulations. Proper biohazard disposal required.

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