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Neogenesis Molding Cog Thread Arrow-Bi 10ea/Pack

$128.00

Neogenesis Molding Cog Thread Arrow-Bi 10ea/Pack​​ utilizes patented bidirectional flat arrowhead barbs with harpoon-shaped notches for unprecedented tissue anchoring. Engineered with medical-grade molding technology, these threads deliver maximal grip strength and 1-5 year lifting efficacy for moderate-to-severe ptosis (grades 1-2) in face, neck, and body.

Quantity discounts
Quantity Discount Price
5-9 3% $124.16
10-19 5% $121.60
20-Unlimited 8% $117.76
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NEOGENESIS MOLDING COG THREAD ARROW-BI

Medically Reviewed & Verified | CE Directive 93/42/EEC |

Advanced bi-directional tissue repositioning system engineered via cold-molding technology. Designed to preserve polymer structural integrity, delivering >45N anchoring force—up to 4x the tensile strength of standard cut threads. Clinically indicated for Grade 1-2 facial ptosis correction, deep fat pad suspension, and subdermal volume vectoring. Stimulates continuous Type I and III collagen neogenesis for sustained 1-5 year tissue support.

Biomechanical Data

Composition: 100% Medical-Grade PCL (Polycaprolactone)

Tensile Strength: >45N (Validated via 9 protocols)

Degradation Profile: Complete hydrolysis at 18-24 months

Barb Architecture: Flat arrowhead & harpoon multidirectional notches

Product Configurations

C19100M-C: 19G W-Blunt / 100mm / 150mm Thread

C18100M-C: 18G W-Blunt / 100mm / 150mm Thread

Packaging: Sterile EO gas double-blister pack (10 units/box)

Storage: 1°C – 30°C, avoid direct sunlight and moisture

Evidence-Based Clinical Protocol

01. Plane of Insertion: Strict sub-SMAS / deep subcutaneous fat layer. Avoid superficial dermal placement to prevent dimpling.

02. Anchor Points: Secure proximal barbs at rigid anatomical landmarks (e.g., dense temporal fascia or preauricular ligaments).

03. Vectors: Define traction vectors based on individual structural deficiency, typically maintaining a 45-degree cephalic angle for midface ptosis.

04. Post-Procedure: Mandate oral antibiotics protocol, cold compress application for 48 hours, and strict limitation of extreme mastication/facial animation for 14 days.

Clinical Safety & Contraindications

Class III Medical Device restricted strictly to licensed medical practitioners. Clinical Study Ref #CT-2023-04 demonstrates a 92% tissue retention satisfaction rate at 24 months. Absolute contraindications include active localized cutaneous infections, severe autoimmune conditions, and uncontrolled coagulopathies. Efficacy and longevity heavily depend on accurate vector planning and baseline tissue volume.

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