SKU: LM15-PRO
Silicone LED Mask with Cryo-Soothe Technology
Combines multi-band phototherapy with precision cooling for rapid post-needling erythema reduction.
Explore SpecificationsEngineered to medical aesthetic standards, featuring calibrated motor output, micro-fluidic delivery channels, and medical-grade bio-compatible contact surfaces.
Combines multi-band phototherapy with precision cooling for rapid post-needling erythema reduction.
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Variable spectrum photodynamic system engineered for post-microneedle biological response activation.
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650nm focused laser diode network designed to amplify micro-injury neovascularization in follicle matrices.
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Ultra-flexible contour matrix delivering uniform 630nm/830nm energy over curved dermal and parietal regions.
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Engineered for medical spa treatments combining active micro-puncturing with soothing transdermal recovery.
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Optimized diode spacing to prevent epidermal hotspots while maximizing ATP synthesis in the follicular bed.
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Industrial clinical-grade thermal dispersion design engineered for intense clinic schedules and durable daily operation.
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Medical grade silicone encapsulated array yielding unmatched flux consistency across the entire scalp arc.
Explore SpecificationsAnalyzing follicular regeneration, microvascular neogenesis, and high-efficiency peptide permeation within clinical practice.
Controlled puncturing via surgical-grade 316/304 stainless steel or titanium micro-needles triggers an orchestrated cascade of platelet-derived growth factors (PDGF), transforming growth factor-beta (TGF-β), and vascular endothelial growth factor (VEGF). This microvascular reconstruction restores nutrient flow directly to dormant dermal papilla cells (DPCs).
Micro-injuries produced at precise needle depths between 0.5 mm and 1.5 mm activate the mechanical transduction sensors in hair follicle stem cells (HFSCs). This physical activation stimulates the canonical Wnt10b/β-catenin pathway, triggering transition out of the telogen phase directly into active anagen follicle morphogenesis.
The scalp's stratum corneum forms a formidable lipid barrier restricting topicals with molecular weights greater than 500 Daltons. OEM motorized derma pen systems create temporary, micro-conduits across this barrier, increasing the bio-availability and systemic delivery of Exosomes, Minoxidil, PDRN, and copper tripeptide-1 up to 800%.
Customized configuration matrix engineered for clinics, trichology studios, and daily home-use scalp treatment protocols.
Professional trichology settings utilize high-frequency digital pens (12,000–18,000 RPM) equipped with disposable sterile 12-pin or 24-pin medical cartridges. Scalp prep protocols use needle depths from 1.0mm to 1.5mm to establish pinpoint bleeding before injecting Autologous PRP or concentrated exosome cocktails, ensuring precise graft vascularization.
Commercial scalp care spaces focus on non-invasive rejuvenation using nano-silicon wafers and 36-pin micro-arrays set to shallow depths (0.25mm–0.50mm). Combined with 650nm LLLT laser therapy caps, these protocols unclog hyperactive sebum follicles and infuse plant-derived stem cells without epidermal bleeding or prolonged client downtime.
Consumer devices feature fixed-depth safety limiters (max 0.5mm), intuitive LED touch controllers, and auto-shutoff fail-safes. Designed for direct consumer distribution, these systems integrate red light phototherapy to maintain anagen follicle vitality between professional clinic visits.
Market segmentation, regulatory updates, and consumer adoption patterns shaping the trichology and aesthetic device industries.
North American buyers prioritize strict FDA 510(k) and 21 CFR Part 820 compliance. The market is shifting from manual dermal rollers to automated, disposable-cartridge pens, driven by safety demands and preventative scalp-care routines among Gen Z and millennial consumers.
The implementation of EU Medical Device Regulation (MDR 2017/745) has increased barrier-to-entry standards across European markets. Brands focus on CE-marked, medical-grade components, biocompability data, and sustainable housing materials to meet stringent distributor guidelines.
In South Korea, Japan, and Southeast Asia, scalp microneedling has integrated directly into comprehensive hair-care regimens. High-frequency automated pens with built-in micro-infusion liquid channels are seeing rapid adoption across specialized scalp spas and boutique clinics.
Combining end-to-end tooling, PCB fabrication, and cleanroom assembly in a streamlined production hub.
By producing CNC-milled metal handpieces, precision eccentric cams, and silicone parts in-house, Fanrun removes intermediate vendor markups. This integration allows rapid prototyping cycles from CAD blueprints to working samples in just 7 to 10 days.
Needle cartridges are assembled and hermetically sealed inside cleanrooms with automated optical inspection (AOI) to eliminate burs, needle dulling, and alignment defects. Every production lot undergoes gamma radiation or ethylene oxide (EO) sterilization with full traceability.
With more than 200,000 square meters of production area and over 100 technicians, our facilities comfortably handle orders ranging from small private-label runs to enterprise batches of 50,000+ units, backed by real-time inventory tracking and rapid logistics links.
Documented outcomes and follicle density evaluations from users of devices built on our hardware platforms.
“My hair has changed dramatically! The previously thinning areas on the top of my head have visibly filled in and look thicker and healthier.”
“I had always been troubled by thinning hair and didn't expect significant changes. The top of my head was very thin before; now the volume has increased a lot.”
“After a few microneedling treatments, my skin has become smoother, scars have improved significantly, and the treatment accelerated regeneration.”
Developing intelligent, sensor-driven scalp therapies to advance next-generation clinical and home treatments.
Integrating pneumatic micro-pumps directly into needle cartridges to automate real-time infusion of peptides and exosomes synced with needle strokes.
Micro-sensors embedded in needle arrays measure scalp epidermal thickness, automatically modulating penetration depth to safeguard vascular layers.
Using optic-fiber core needle tips to transmit 650nm coherent light into the hair follicle base during physical puncturing, accelerating cellular repair.
Pens with high-resolution digital cameras assess follicle density and sebum levels, pairing with mobile apps to adjust treatment speeds in real time.
All aesthetic and scalp systems hold CE and RoHS documentation, and skin-contact materials are verified food-grade by TUV and SGS.
Full adherence to EU low-voltage and electromagnetic compatibility directives for medical and beauty appliances.
Free of hazardous substances, heavy metals, and toxic chemical coatings on all circuit boards and contact housings.
Rigorous cytotoxicity, sensitization, and biocompatibility verification for surgical steel needles and silicone materials.
Proprietary motor mechanics, precision anti-backflow needle designs, and thermal dispersion architectures protect your brand.
A structured 6-stage engineering path from concept validation to reliable batch shipment.
We review your regulatory market, target price points, depth needs (0.25mm–2.5mm), motor RPM profiles, and packaging preferences.
Our engineers draft 3D mockups, customize needle cartridge fittings, design circuit layouts, and calibrate custom speed indicators.
Functional working prototypes are CNC-machined and assembled within 7-10 business days for mechanical testing and client sign-off.
We prepare CE, RoHS, and FCC test files, assemble material declarations, and assist partners with regional import clearance requirements.
Scalable high-volume production using automated surface-mount PCB lines, cleanroom needle assemblies, and batch-coded production lots.
Every unit undergoes battery cycle tests, motor RPM checks, and pre-shipment inspections before secure overseas export.
Reliable platforms ready for rapid customization, branding, and global commercial launch.
Combines 415nm, 590nm, 630nm, and 830nm NIR diodes to soothe scalps and support cellular regeneration.
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Our flagship pen featuring a high-torque coreless motor, 5-speed digital dial, and needle adjustments from 0.00 to 2.50mm.
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High-density coherent red diode layout provides complete coverage to rejuvenate dormant hair roots.
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Skin-safe silicone mask tested by TUV/SGS to ensure irritation-free post-needling phototherapy care.
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Lightweight, baseball cap-compatible wearable laser system designed for regular at-home compliance.
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Durable aerospace-aluminum chassis engineered for clinical treatments, chemical peel prep, and trichology procedures.
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Patented silicone diaphragm design prevents fluids and blood backflow into the handpiece, protecting against contamination.
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Features adjustable pulse frequencies that promote microvascular healing without thermal buildup on sensitive scalps.
View Product DetailsClear, direct answers regarding production limits, regulatory requirements, sterilization methods, and custom development.
Yes. Fanrun supports comprehensive OEM private label programs (laser-etched logos, custom housing colors, packaging, user manuals) and full ODM development (custom injection tooling, LED PCB layouts, wavelength combinations, firmware modifications, and app connectivity) across all product families.
Our aesthetic and medical platforms carry full CE (EMC and LVD directives) and RoHS compliance. All patient/skin-contact materials—including medical-grade liquid silicone and 316 surgical steel needles—pass food-grade safety and cytotoxicity testing certified by TUV and SGS. Complete test dossiers are made available to verified brand partners on request.
For hair regrowth and follicle stimulation, we specialize in high-output 650nm low-level laser (LLLT) and 630nm/830nm near-infrared LED arrays. Custom combinations—including 415nm blue light to treat scalp microflora and oil build-up, and 590nm yellow light to reduce swelling—can be engineered to match your protocol.
We encourage thorough due diligence. Our sales representatives provide active certification tracking numbers and testing records, which can be verified directly through official online portals at TUV Rheinland and SGS.
MOQ varies by customization level: logo-only private labeling typically starts at 200–500 units, while customized body colors, new cartridge designs, or full ODM shell modifications begin at 1,000–3,000 units. Working samples ship in 7 to 10 days, and full mass production runs complete in 25 to 35 days.
Our cartridges incorporate a medical silicone barrier membrane that forms a hermetic seal behind the needle drive. This prevents topical serums, blood, or lymphatic fluid from moving back into the pen handpiece, protecting against cross-client contamination and extending internal motor life.
Request technical specifications, test reports, and factory direct quotes. Our Shenzhen engineering team provides end-to-end guidance from initial CAD concepts through to final certification.
To verify authenticity, request the certificate number from our team and check it on the issuing body's official portal. Contact us