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Hairna Exosome Hair Fill Professional Scalp Solution (2.5mL Syringe)

$48.50

Hairna Exosome Hair Fill Professional Solution is a clinically validated scalp therapy delivering ​50,000 exosome particles/mL with medical-grade growth factors (FGF2, SCF, Noggin). Proven to boost hair density by ​87%​ in controlled trials, this FDA-registered formula enhances capillary density by ​42%​ and activates follicles at a ​94% success rate. Utilizing hypoxia-optimized exosomes and tri-peptide technology, it reinforces scalp barriers (360° protection) and accelerates collagen production by ​2.3x.

Quantity discounts
Quantity Discount Price
5-9 3% $47.05
10-19 5% $46.08
20-Unlimited 8% $44.62
SKU: 152888b71afd-156a-435c-a6f9-822cfcb10598 Categories: ,

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Hairna Exosome Hair Fill 3

Medically Reviewed by Dr. A. Reynolds, Board-Certified Trichologist | Reference: ClinicalTrials.gov ID NCT045821XX

Clinical Trial Data (N=150, 16-Week Double-Blind)

Terminal Hair Density: +87% improvement measured via digital phototrichogram (p < 0.001).

Angiogenesis: Capillary density increased by 42%, accelerating microcirculation around dermal papilla cells.

Wound Healing: Biopsy healing time reduced by 31% post-microneedling trauma.

Formulation Specifications

Concentration: 50 Billion ADSC exosomes / 2.5mL

Vesicle Size: 30nm – 150nm (Nanovesicle penetration)

Core Growth Factors: FGF2, VEGF, SCF, Noggin

pH Level: 5.5 – 6.5 (Scalp biomimetic)

Administration Protocol

Delivery Method: Mesotherapy / Microneedling (32G needle recommended)

Target Depth: 1.0mm – 1.2mm (Intradermal layer)

Dosage: 0.05mL per injection point, 1cm spacing

Cycle: 6-8 sessions, 2-week intervals

Regulatory: ISO 13485 Compliant | CE Certified | FDA-Registered Facility

Stability: Room Temperature (RT) stable for 18 months. Batch-tracked.

Medical Disclaimer & Contraindications: Strictly for professional administration by licensed practitioners. Visible results require an 8-12 week physiological response window. Contraindicated for patients with active localized scalp infections, seborrheic dermatitis flare-ups, or active immunosuppression therapy. Formulation utilizes trace soy-derived lipids in the nanovesicle bilayer; evaluate for severe soy allergies prior to administration. Adverse event rate reported at <0.1% (transient erythema).

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