Neogenesis PDO Mono Thread
Medical-Grade Bio-Stimulation
Advanced Polydioxanone (PDO) monofilament technology engineered for subdermal tissue remodeling. Utilizing USP 6-0 gauge precision (Ø0.07-0.1mm), these threads induce a controlled foreign body reaction, triggering Neocollagenesis in the SMAS and dermal layers.
ISO 13485 Certified
CE Marking
Efficacy Data: 47% reduction in perioral rhytids and 29% improvement in dermal density verified via high-frequency ultrasound imaging over a 90-day clinical observation period.
Technical Specifications
Material Longevity
Biodegradable Polydioxanone polymer. Full hydrolytic absorption occurs between 180–240 days via non-enzymatic cleavage.
Tensile Strength
High-retention monofilament design. Superior knot strength and flexibility ensures zero breakage during 30° vector implantation.
Cannula Geometry
Ultra-thin wall (UTW) L-Type or U-Type cannula options. Siliconized surface coating reduces insertion resistance by 15%.
Dermatological Evidence & Safety
| Parameter | Clinical Metric | Observed Result |
|---|---|---|
| Collagen Type | Type I & Type III | Regenerative Neocollagenesis |
| Tissue Reaction | Myofibroblast Activation | Immediate Mechanical Tightening |
| Safety Class | KFDA / Class II Device | Non-pyrogenic, Sterile (EO Gas) |
Contraindications & Professional Warning
Strictly prohibited for patients with keloid predisposition, active cutaneous infections, or systemic autoimmune disorders. This product is intended for professional use only by certified practitioners. Unauthorized application may result in granuloma, nerve damage, or vascular compromise.

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