Select fully tooling-validated, certified medical aesthetic platforms engineered for rapid institutional and retail private-label rollout.
Post-CIT soothing system combining dual cryo-cooling with medical phototherapy (415nm-830nm) for accelerated dermal remodeling.
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Professional multi-spectrum facial canopy targeting localized dermal fibroblasts post-microneedling channel perforation.
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Engineered for scalp CIT protocols; combines mechanical follicle stimulation with concentrated coherent diode arrays.
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Bendable clinical-grade high-irradiance array (630nm/830nm) delivering deep therapeutic photons following CIT therapy.
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Surgical stainless chassis, high-torque micro-stepping core, and anti-backflow fluidic safety cartridge compatibility.
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SGS/TUV biocompatible food-grade silicone contact layer engineered for clinical hygiene and high-output photon immersion.
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Dual wireless induction docking, 0.20mm - 2.50mm dial precision depth control, calibrated at 16,000 RPM puncture speed.
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Omni-directional coverage designed specifically for trichology practices combining scalp epidermal puncture with low-level laser.
Explore SpecificationThe international aesthetic medicine sector is transitioning rapidly from abrasive chemical peels and ablative fractional lasers to precision micro-mechanical Collagen Induction Therapy (CIT). Enterprise buyers, dermatological chains, and tier-1 cosmetic brands require reliable OEM/ODM partners capable of strict mechanical repeatability.
Controlled mechanical micro-injuries trigger a natural wound-healing cascade without thermal coagulation of adjacent tissues. Platelet-derived growth factors (PDGF), transforming growth factor-beta (TGF-β), and fibroblast growth factor (FGF) activate neo-collagenesis and neo-elastinogenesis in the reticular dermis.
Global distributors are abandoning fragmented trading firms in favor of factory-direct partnerships. Critical procurement parameters now prioritize needle deflection tolerances below 0.02mm, strict gamma/EO sterilization protocols, and comprehensive technical documentation for cross-border customs approval.
Cross-contamination risks have catalyzed strict regulatory mandates worldwide. Shenzhen Fanrun Technology engineers proprietary integrated anti-backflow silicone membranes within each single-use needle cartridge, completely isolating fluid aerosols from the motor drive shaft.
Shenzhen Fanrun Technology Co., Ltd. (Est. 2013) combines in-house industrial tooling, cleanroom cartridge assembly, surface metallurgy, and robotic micro-stepping motor calibration.
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Patents Granted
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Surgical Grade 316L medical stainless steel and optional titanium nitride coatings ensure zero burring and painless epidermal entry.
High-RPM magnetic coreless stepping motors designed for pure vertical reciprocating motion, preventing epidermal scratching or tearing.
TUV and SGS certified skin-contact silicone and aircraft-grade aluminum alloy with medical electroplating resistant to chemical disinfectants.
Batch tracking from raw metal wire drawing to sterile blister packaging, complete with inspection certificates matching ISO standards.
Direct data reported by licensed clinicians and private label brand partners using Fanrun OEM Collagen Induction Therapy devices and auxiliary photobiomodulation platforms.
High-frequency mechanical puncture creates over 1,000 micro-conduits per second without stripping the protective stratum corneum. Clinical biopsies display marked upregulation of Type I and Type III pro-collagen messenger RNA within 48 hours post-treatment.
Shenzhen Fanrun R&D centers are pioneering multi-modal convergence. Here is how our engineering laboratory is leading the future of automated microneedling technology.
Integrating real-time epidermal resistance sensors into the cartridge tip. The onboard micro-controller algorithmically adjusts reciprocating stroke length based on local tissue density (forehead vs. cheek), preventing periorbital bone strikes and ensuring uniform dermal target delivery.
Transitioning from passive topical application to precision peristaltic micro-dosing. Automated pneumatic channels release precise nanoliter volumes of exosomes, hyaluronic acid, and peptide complexes synchronously with needle retraction.
Insulated gold-plated micro-pins delivering localized thermal coagulation strictly at the reticular dermal plane while preserving epidermal barrier integrity, bridging the gap between mechanical CIT and aesthetic laser systems.
Cleanroom micro-molding tooling tailored for high-molecular weight cross-linked hyaluronic acid microneedle patches, providing needleless deep subcutaneous active compound bioavailability.
We eliminate regulatory bottlenecks for importers. Fanrun products hold CE Class I / IIa declarations, RoHS 2.0 directive compliance, and comprehensive SGS/TUV testing records covering biocompatibility and safety.
CE CONFORMITY DIRECTIVE
RoHS 2.0 HAZARD SCREENING
TUV BIOCOMPATIBILITY TEST
SGS FOOD-GRADE SILICONE
Full lifecycle support ensuring institutional engineering, customized injection tooling, firmware programming, and rapid scale.
Aligning needle counts, motor speeds, mechanical stroke lengths, custom enclosures, and target jurisdiction clearance pathways.
Tooling of custom ergonomics, fluidic reservoir housings, battery containment, and high-frequency tactile switches.
Custom speed curve presets, battery monitoring algorithms, digital LED indicators, and Bluetooth telemetry for companion skincare applications.
Single-use needle cartridge assembly executed under controlled atmospheric cleanliness, backed by ethylene oxide (EO) sterilization validation.
Automated optical inspection (AOI) guarantees needle tip sharpness, straightness, and zero burrs before sealing.
Complete packaging with multi-language instruction manuals, test reports, UN38.3 lithium battery flight certifications, and DDP shipping.
Order directly from validated active product lines or initiate custom white-label branding.
Integrated solid-state cryo-plates reduce post-procedure erythema while 830nm NIR stimulates localized cellular ATP generation.
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Broadband therapeutic coverage designed to accompany microneedling protocols in medical spa settings.
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Targeted 650nm high-density laser diodes configured for synergy with scalp micro-needling trichology therapies.
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Durable, fully articulated multi-positional array for intensive collagen activation across the face, neck, and décolleté.
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Single-use configurations available in 12, 24, 36, 42 pins and nano-arrays, individually gamma sterilized with safety membrane seals.
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Soft-touch silicone base integrating red and near-infrared chips designed to optimize scalp perfusion before mechanical CIT treatments.
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Features ultra-low acoustic decibel operation, ergonomic anodized grip, and continuous linear vertical reciprocating action.
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TUV/SGS non-cytotoxic certified silicone mask configured with customized industrial wavelengths for enterprise aesthetic brands.
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Yes. We provide complete OEM (logo laser-etching, custom pantone finishing, specialized user manuals, gift packaging) and full ODM industrial development. Our ODM capabilities include custom tooling for handpiece shells, micro-motor RPM tuning, stroke length customization (up to 2.5mm), fluidic cartridge mold development, and custom printed circuit board assembly (PCBA) with Bluetooth or LCD touchscreen logic.
Our single-use cartridges are engineered with an integrated medical-grade silicone diaphragm barrier. This hermetic membrane creates a physical seal between the reciprocating drive shaft and the needle fluid reservoir, completely blocking biological fluids, blood, and cosmetic serums from entering the handpiece motor cavity.
All Fanrun CIT and phototherapy devices carry CE and RoHS certifications. Skin-contact components (including medical silicone masks and housing materials) have undergone food-grade and non-cytotoxicity testing certified by TUV and SGS. We supply verified test reports, CE declarations of conformity, and UN38.3 battery flight documentation directly to our purchasing partners.
For custom private label (customized packaging, pantone color selection, and silk-screened logos on standard platforms), our MOQ typically begins at 500 to 1,000 units. For full ODM projects requiring custom injection tooling and unique housing architecture, initial runs start at 2,000 to 3,000 units. Standard production lead times average 25–35 days following prototype sign-off.
Every needle batch undergoes automated optical inspection (AOI) to eliminate hooks, burrs, or dimensional deviations. Needle points are milled from medical 316L stainless steel or titanium, ensuring high structural integrity and clean vertical penetration without the micro-shearing or epidermal gouging common in substandard cast rollers.
Absolutely. While our standard setups utilize clinical wavelengths such as 415nm (anti-microbial blue), 590nm (soothing yellow), 630nm (collagen stimulating red), and 830nm (deep penetrating near-infrared), our optoelectronics engineers can calibrate LED density, radiant intensity (mW/cm²), and custom narrow-band spectrums according to your institutional requirements.
Eliminate trading company markups, secure batch consistency, and accelerate time-to-market with Shenzhen Fanrun Technology.
To verify authenticity, request the certificate number from our team and check it on the issuing body's official portal. Contact us
