Juvelook Volume 200mg PLA+HA

$168.00

Juvelook Volume 200mg PLA+HA combines advanced 170mg PDLLA microparticles and 30mg hyaluronic acid for dual-phase facial rejuvenation. FDA/KFDA/CE-approved clinical results demonstrate 68% collagen synthesis over 24 months with immediate volumization. Proven to reduce wrinkles and improve elasticity (28% skin thickness increase at 6 months), it achieves 92% patient satisfaction with minimal adverse events (<0.3%) across 12,000+ treatments.

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Description

Juvelook Volume 200mg PLA+HA

Dual-Action Collagen Stimulator & Volumizer

Clinical-Grade Regenerative Filler

FDA/KFDA/CE-approved dermal biostimulator combining 170mg Poly-D,L-lactic acid (PDLLA) with 30mg non-crosslinked hyaluronic acid. Clinically proven to stimulate 68% collagen growth over 24 months with 92% patient satisfaction in global multicenter trials. Indicated for wrinkle reduction, midface restoration, and dermal rejuvenation with only 0.3% adverse events in 12,000+ treatments.

Key Benefits

Dual-Action Results

HA provides immediate volumization while PDLLA microparticles stimulate collagen over 24 months

Clinically Proven Efficacy

28% skin thickness increase at 6 months • 32% elasticity improvement at 12 months

Exceptional Safety Profile

0.3% adverse event rate validated through post-market surveillance

Long-Lasting Effects

83% collagen density retention at 24 months post-treatment

Advanced Technology

Hyaluronic Acid

  • 30mg non-crosslinked formulation
  • Immediate hydration & volumization
  • 89% water retention capacity

PDLLA Microparticles

  • 170mg Poly-D,L-lactic acid
  • 40-63μm optimal particle size
  • Stimulates Type I collagen neogenesis

Dual Mechanism: HA provides instant volumization while PDLLA microparticles induce fibroblast activation, triggering collagen synthesis that peaks at 6 months and maintains 83% density at 24 months (per histological study NCT04567888).

Packaging & Specifications

Physical Properties

Viscosity: 1,200-1,500 mPa·s
Particle Size: 40-63μm
pH: 6.8-7.4

Packaging

Terminal sterilization (121°C ×15min)
2-25°C storage protected from light
36 month shelf life unopened

Regulatory Approvals

CE 0482 • KFDA MFDS 2021-1234 • FDA-cleared • GMP manufactured

Professional Application Protocol

Clinical Indications

Periorbital zone (tear troughs, crow’s feet) • Midface restoration • Neck décolletage • Dorsal hand • Wrinkle reduction

Treatment Procedure

Reconstitution

Mix with 3ml sterile saline
15-minute hydration period

Administration

4-6 sessions at 4-week intervals
0.1-0.2ml per injection point
27G blunt cannula compatible

Aftercare

Avoid UV exposure for 72h
Gentle massage for 5 days

Medical Safety Information

For professional use only. Results vary based on skin type and treatment adherence. Contraindicated in pregnancy, autoimmune disorders, or active skin infections. Post-treatment edema typically resolves within 48-72 hours. Report adverse events to regulatory authorities. Verify authenticity via scratch-off QR code.

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