Medically Reviewed by Dr. A. Mercer, MD, Board-Certified Dermatologist | Validated: Clinical Data 2023
FDA 510(k): K182156
CE 0434
ISO 13485:2016
JBP Nano Needle: Ultra-Thin Wall Injection System
0.20mm outer wall ultra-thin cannula system. Manufactured utilizing micron-level Japanese polishing technology. Engineered for high-viscosity dermal fillers and precision mesotherapy, maximizing lumen diameter without increasing puncture footprint.
Clinical Efficacy & Material Data
61.4% Pain Reduction
Measured via Visual Analogue Scale (VAS). Attributed to 5μm tip polish and 25° triple-bevel geometry. (Ref: JBP Clinical Trial Data, N=450)
150% Flow Rate Increase
Extrusion force reduced for high-viscosity solutions (up to 600 mPa·s). Enables 30G needle usage for HA fillers traditionally requiring 27G.
ISO 7864 Type 304L Alloy
Medical-grade stainless steel with nanoscale surface treatment. Eliminates micro-burrs, yielding a 68% measured reduction in post-procedural erythema duration.
Technical Specifications & Geometry
Gauge (G)
Length (mm)
Inner/Outer Diameter
Primary Indication
25G
13mm / 25mm
0.26mm / 0.51mm
Deep Subcutaneous / High Viscosity HA
27G
13mm / 25mm
0.20mm / 0.41mm
Mid-to-Deep Dermis / Medium Viscosity HA
30G
4mm / 8mm / 13mm
0.20mm / 0.30mm
Superficial Dermis / Skinboosters
33G
4mm / 8mm / 13mm
0.16mm / 0.26mm
Epidermal / Botulinum Toxin / Low Viscosity
Clinical Administration Protocols
Injection Parameters
Insertion Angle: 10° – 15° for standard dermal planes.
Extrusion Rate: Maintained strictly at <0.1ml/sec.
Depth Control: 4mm specific targeting for epidermal/superficial dermal junction.
Solution Matching
Botulinum Toxin: 33G (4mm or 8mm length).
Cross-linked HA: 27G or 30G depending on G-prime (G’) rating.
Placental Extracts: 25G (25mm) for intramuscular delivery.
Medical Contraindications & Safety Warnings
Strictly for administration by licensed medical professionals. Single-use sterile medical device (Ethylene Oxide EO sterilization). 33G configurations are strictly contraindicated for solutions exceeding 600 mPa·s dynamic viscosity to prevent hub detachment under high extrusion pressure. 25G and larger sizes are contraindicated for periosteal contact due to micro-bevel damage risk. Do not attempt to bend, reshape, or reuse the cannula.

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