SKU: LM15
Anti-Aging 4 Colors Light Therapy Ice Function Silicone Mask
Engineered for deep dermal recovery, incorporating integrated cryo-soothing modes and medical-grade bio-compatible contact silicone.
View SpecificationsExplore production-ready OEM/ODM hardware platforms engineered in-house with clinical calibration, high-grade motor logic, and complete certification portfolios.
Engineered for deep dermal recovery, incorporating integrated cryo-soothing modes and medical-grade bio-compatible contact silicone.
View Specifications
Multi-spectral photodynamic matrix configured for institutional skin rejuvenation, blemish mitigation, and controlled cellular stimulation.
View Specifications
Medical 650nm LLLT diode dispersion system configured for scalp microcirculation enhancement and thinning hair treatment.
View Specifications
Flexible contouring light therapy architecture engineered for ergonomic face and neck application using calibrated 630nm/830nm arrays.
View Specifications
High-torque micro-motor pen with digital rpm display, anti-backflow sterile cartridge locking system, and dual wired/wireless logic.
View Specifications
High-frequency clinical dermal perforation system featuring micro-depth dial adjustment (0.25mm - 2.50mm) for dermatology suites.
View Specifications
Contoured phototherapy device with targeted wavelengths targeting fibroblasts, collagen synthesis, and post-procedural swelling.
View Specifications
Multi-purpose wearable red light wrap engineered for targeted scalp follicle activation and post-microneedling dermal repair.
View SpecificationsThe global transdermal delivery and minimally invasive aesthetic device ecosystem is experiencing rapid structural maturity, driven by stringent regulatory frameworks and shifting clinic procurement behaviors.
Global distributors, dermatology clinics, and medspas require strict adherence to medical device stability. Needle depth tolerance must not deviate beyond ±0.03mm under sustained pressure. Sourcing teams prioritize direct manufacturers capable of demonstrating motor longevity testing exceeding 1,200 continuous run hours.
The industry benchmark is defined by anti-backflow fluid isolation barriers. Single-use needle cartridges require medical-grade polycarbonate housings and medical stainless steel (304/316L) needles subjected to gamma-ray or EO sterilization, eliminating risk of cross-contamination.
Tier-1 importers require end-to-end component traceability. From raw titanium/aluminum CNC lathe operations down to PCB surface-mount assembly (SMT), every lot is indexed with batch control codes to simplify customs clearing and national health ministry registrations.
Fanrun Technology operates an integrated 200,000+ m² production facility with in-house industrial tooling, cleanroom assembly lines, and proprietary motor calibration labs.
We eliminate skin dragging and tearing through customized coreless micro-motors capable of generating 8,000 to 18,000 RPM with pure vertical needle impact. This minimizes epidermal micro-trauma and accelerates client recovery periods across all skin phototypes.
Our dial mechanisms utilize stepped spiral slot engineering calibrated down to micrometric increments. With zero-slip mechanical detents at 0.25mm intervals, practitioners operate with absolute assurance of targeted depth into the papillary dermis.
We design sterile multi-pin needle cartridges ranging from 9-pin, 12-pin, 24-pin, 36-pin, 42-pin to round and square nano-silicon arrays. Every cartridge features an integrated silicone elastomer diaphragm preventing serum backflow into the handpiece drive core.
As micro-needling transitions from mechanical puncture into active drug delivery and energy-assisted tissue remodelation, Fanrun Technology leads the hardware innovation curve with next-generation patents.
Development of isolated needle pins with bipolar radiofrequency energy delivery focused strictly at the needle tip, inducing thermal coagulation in the reticular dermis while sparing the epidermis from thermal injury.
Engineering synergistic handpieces combining physical micro-perforation with transdermal electroporation pulses, enhancing macromolecular bioavailability (hyaluronic acid, exosomes, peptides) by up to 400%.
Synchronized optical output directly built into derma pen handpieces, deploying simultaneous 415nm (anti-inflammatory) and 630nm (collagen boost) irradiation directly onto open micro-conduits during puncture.
Next-generation derma pen consoles with micro-Bluetooth telemetry recording procedural duration, needle depth, speed profiles, and cartridge serial verification for tamper-evident medical record keeping.
Shenzhen Fanrun Technology Co., Ltd. operates an integrated aesthetic hardware facility with complete in-house tooling, cleanroom injection, assembly, and testing.
Every motorized pen, battery charging base, and optical accessory passes comprehensive electromagnetic compatibility (EMC) and low-voltage directive (LVD) assessments for risk-free importation across the EU.
All direct contact points—including anodized aircraft aluminum, silicone eye covers, and face shields—undergo rigorous food-grade and cytotoxicity safety screenings certified by TUV and SGS testing labs.
No intermediaries or sourcing brokers. Your engineering parameters are discussed directly with our optical, mechanical, and firmware engineers, ensuring rapid DFM reviews and reliable batch production.
From initial design intent to national border clearance, Fanrun provides an institutional six-stage structured manufacturing lifecycle.
Definition of clinical scope, targeted puncture depth, battery capacity (300mAh - 800mAh), motor RPM specs, custom color palettes, and retail packaging configurations.
Mechanical design, shell injection molds, PCB schematics, and cartridge locking mechanism development backed by Rapid-DFM structural analysis.
CNC precision prototyping, vibration dampening testing, needle deflection analysis, and aesthetic surface treatments (matte, metallic anodizing, PVD).
Preparation of factory test logs, EMC/LVD reports, biocompatibility documentation (TUV/SGS), and CB scheme certificates to expedite importer registration.
Automated cleanroom assembly, strict inward material inspections (IQC), in-process quality control (IPQC), and serial batch printing.
100% full-cycle run-in testing, battery load capacity assessment, drop tests, packaging drop simulations, and verified export logistics support.
Authoritative technical answers to primary procurement queries raised by medical device buyers, brand developers, and regulatory officers.
Yes. Fanrun provides complete OEM private label solutions (logo laser engraving, housing color anodization, custom packaging boxes, multilingual manuals) as well as comprehensive ODM development (custom handpiece industrial design, proprietary PCB motor controller design, custom needle cartridge mold fabrication, and optical wavelength configurations).
Our aesthetic and microneedling devices comply with CE (EMC/LVD), RoHS, and FCC directives. Handpiece skin-contact materials and flexible silicone masks have completed and passed rigorous biocompatibility and food-grade non-toxicity testing certified by third-party testing organizations including TUV and SGS. Complete test reports and declarations of conformity are provided to buyers upon request.
Needle dragging occurs when a pen operates with insufficient motor torque or loose mechanical axial tolerances. Fanrun derma pens use customized German-engineered coreless micro-motors operating between 8,000 and 18,000 RPM, paired with linear guide linkages. This ensures rapid vertical puncturing with microsecond retraction speeds, preventing lateral tissue shearing during handpiece translation across the skin.
We champion anti-counterfeiting transparency. When evaluating our factory credentials, request the individual certificate or technical report registration numbers from our dedicated sales team. You can verify these credentials directly through official online validation portals operated by TUV Rheinland, SGS, or respective European Notified Bodies prior to contract signing.
MOQ varies based on customization level. For silk-screen or laser-marked private label orders on existing stock platforms, MOQs typically begin at 100 to 500 units with 15–20 day fulfillment. For bespoke ODM projects requiring custom CNC housings, custom PCB programming, or proprietary cartridge tooling, MOQs generally start at 1,000 units with tooling turnaround in 30–45 days followed by volume batch production.
Explore our specialized portfolio of clinic-ready micro-needling platforms, phototherapy systems, and post-procedure clinical units built for volume distribution.
Four-spectrum targeted phototherapy platform combining integrated cooling modules for comprehensive post-microneedle recovery.
View Specifications
Comprehensive optical wavelength management device engineered for acne care, pore reduction, and tissue recovery programs.
View Specifications
High-density 650nm low-level laser therapy device designed for targeted, full-scalp thinning hair restoration routines.
View Specifications
Ergonomic, wrap-around silicone panel utilizing medical-grade 630nm and 830nm near-infrared arrays for face and neck repair.
View Specifications
Lightweight wearable design featuring even light dispersion and food-grade silicone contact testing for sensitive skin treatments.
View Specifications
Targeted scalp revitalization platform featuring smart timed cycles and high-efficiency diode output for home and clinic care.
View Specifications
Calibrated 830nm near-infrared and 630nm red light spectrum for promoting accelerated fibroblast activation and collagen density.
View Specifications
Full compliance testing files, safety evaluations, electrical EMC reports, and custom OEM packaging layout resources.
Download CatalogConnect directly with Shenzhen Fanrun Technology's engineering and export compliance group for wholesale tiered pricing, ODM sample requests, and technical dossiers.
To verify authenticity, request the certificate number from our team and check it on the issuing body's official portal. Contact us