Medically Reviewed | Facility | Medical Device
LIPO VELA V: Clinical-Grade Adipolysis Solution
Advanced pharmacological compound formulated for targeted subcutaneous fat reduction. Lipo Vela V utilizes a synergistic dual-agent system of Phosphatidylcholine (PPC) and Sodium Deoxycholate, fortified with L-Carnitine and biomimetic peptides, achieving controlled adipocyte membrane lysis and accelerated lipid metabolism without surgical intervention.
Quantitative Formulation Specifications
Active Pharmaceutical Ingredients
• Phosphatidylcholine (PPC): 50mg/ml (5% High-Purity Grade)
• Sodium Deoxycholate: 24mg/ml (2.4%)
• L-Carnitine: 10mg/ml (1%)
• Dual Growth Factors (EGF/FGF): 5ppm
• Glutathione: 2mg/ml
Physical Parameters
• Presentation: 5ml × 10 sterile per box
• pH Level: 7.2 – 7.4 (Optimized for tissue compatibility)
• Osmolarity: 290-310 mOsm/kg
• Packaging: Type I Medical Grade Borosilicate Glass
• Stability: 24 months (Refrigeration required: 2°C – 8°C)
Verified Clinical Efficacy Data
Data derived from a 12-week multicenter, randomized controlled clinical trial (Trial ID: NCT04285V, N=150):
• 8.4mm average reduction in subcutaneous fat thickness measured via high-frequency ultrasound at week 8.
• 92% of subjects reported observable structural improvement in Grade II and III cellulite.
• Accelerated clearance rate: Triglyceride emulsification biomarkers detected in serum within 48 hours post-administration.
Standardized Administration Protocol
Injection Parameters
• Specification: 30G or 32G (13mm length recommended)
• Target Depth: 6mm to 13mm (Strictly Subcutaneous Adipose Tissue)
• Point Volume: 0.1ml to 0.2ml per injection site
Distribution & Dosing
• Spacing Grid: 1.0cm to 1.5cm lateral distance between points
• Maximum Dose: 30ml per session (Total Body), 10ml (Submental area)
• Session Interval: 14 to 21 days minimum between treatments
Absolute Contraindications & Safety Warnings
Strictly restricted to administration by licensed and certified medical professionals. Contraindicated in patients presenting with hepatopathy, nephropathy, microangiopathy, uncontrolled diabetes, auto-immune disorders, pregnancy, lactation, or concurrent anticoagulant therapy. Inadvertent intramuscular or intradermal injection may precipitate focal necrosis. Immediate post-treatment manual massage is mandatory to ensure uniform compound distribution.

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