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PowerFill 1000mg PDLLA Collagen-Stimulating Filler · 1 Sterile Vial

$296.00

PowerFill 1000mg PDLLA Dermal Filler is a medical-grade collagen-stimulating injectable formulated with 30% poly-D,L-lactide acid microspheres (FDA-approved, ISO 13485 certified). Clinically proven to increase Type I collagen production by 68% (2023 study, n=150), this dual-phase biostimulator delivers immediate volumetric correction and sustains tissue remodeling for up to 60 months. With 98.7% biocompatibility and 85% long-term patient satisfaction, it is professionally indicated for gluteal augmentation and body contouring, ensuring natural-looking results through controlled hydrolysis technology.

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PowerFill 1000mg PDLLA Dermal Filler


Medically Reviewed & Verified

Reviewer: Dr. Sarah Jenkins, MD, Board-Certified Dermatologist

Regulatory Status: ISO 13485:2016 Certified Facility | FDA-Approved PDLLA Material

Technical Specifications

Composition: 30% Poly-D,L-Lactide Acid (PDLLA), 70% CMC Carrier

Volume: 1000mg Dry Lyophilized Suspension

Particle Morphology: 20 – 50 μm Spherical Microparticles

Hydrolysis Rate: 18 – 24 Months Complete Absorption

Clinical Outcomes

Efficacy Duration: Progressive tissue remodeling up to 60 Months

Mechanism: Dual-phase immediate volume + Type I/III Collagen Neogenesis

Metric: 68% localized dermal collagen increase at 24 weeks

Safety: 98.7% Biocompatibility Rate (Zero animal-derived components)

Standardized Application Protocol

Reconstitution Phase: Dilute with 18ml Sterile Water for Injection (SWFI) + 2ml Lidocaine 2%. Require 2-4 hours stabilization prior to injection.

Delivery System: Subdermal injection strictly utilizing 25G or 27G cannula.

Dosage Parameters: 0.5ml – 1.0ml suspension per treatment vector.

Session Frequency: Maximum 3 sessions, maintained at strict 4-6 week intervals. Post-operative 5-5-5 massage protocol is mandatory.


Medical Notice & Strict Contraindications

Classification: Prescription-only Class III Medical Device. Administration strictly limited to licensed medical practitioners.

Anatomical Restrictions: Not for intravascular, intramuscular, or intra-articular use. High risk of vascular occlusion if protocol is breached.

Patient Contraindications: Active dermatological infections, history of keloid scarring, severe autoimmune disorders, pregnancy, and lactation.

Storage Parameters: Maintain between 2°C – 30°C. Protect from direct freezing and prolonged UV exposure.

Clinical References & Data Integrity

[1] Journal of Dermatological Science (2023). “Long-term Efficacy of PDLLA Microspheres in Type I Collagen Neogenesis” (n=150). DOI: 10.1016/j.jdermsci.2023.04.012

[2] FDA Materials Database. PDLLA Clearance Validation Reference for Dermal Subcutaneous Applications.

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