Validated clinical and med-spa devices manufactured under strict ISO 13485-aligned cleanroom tolerances with customized firmware options.
Flexible food-grade silicone facial platform with active ice soothing module designed for post-microneedling erythema reduction.
High-density optical diode configuration calibrated for deep collagen induction therapies and post-exosome micro-channel recovery.
650nm low-level laser diode therapy engineered for scalp micro-circulation and synergistic scalp microneedling protocols.
Ergonomic high-yield bendable matrix suited for face, neck, and décolleté rejuvenation protocols in clinical environments.
A strategic overview of clinical demand drivers, regulatory governance under HSA, and high-performance device requirements.
Singapore’s Health Sciences Authority (HSA) imposes strict medical device classification parameters. Automated derma pens breaching the epidermis require zero needle-wobble, anti-backflow silicone check valves, and ISO 10993 cytotoxicity compliance to prevent patient cross-contamination.
Aesthetic clinics along Orchard Road and Novena Medical Centers have shifted toward advanced mesotherapy cocktail infusions (Salmon DNA/PDRN and plant/adipose-derived exosomes). This requires ultra-precise needle penetration depth adjustment (0.25mm to 2.50mm) to deliver actives accurately into the basal membrane.
As ASEAN’s premier medical hub, Singapore clinics cater to regional international patients from Indonesia, Malaysia, and Vietnam who demand minimal downtime treatments. Medical-grade engineering ensures uniform epidermal punch without epidermal tearing, reducing erythema from days to hours.
From custom CNC aircraft-grade aluminum handles to micro-motor PWM stability circuits, Fanrun delivers turnkey factory integration for global procurement teams.
Our automated microneedling pens utilize high-speed coreless motors delivering up to 18,000 RPM with low mechanical resonance. This guarantees vertical puncturing without skin dragging, minimizing micro-tears and client discomfort during deep dermis treatments.
Cartridge engineering incorporates medical-grade surgical 304/316 stainless steel needles and a dual-silicone safety membrane barrier that physically prevents blood and serums from entering the handpiece shaft, fully complying with clinical infection-control mandates.
We provide comprehensive corporate customization: anodized housing pantone matching, custom speed LCD firmware, tailored sterile blister pack design, and localized international power adaptations (Type G plug standard for Singapore and UK distribution).
Evaluation of clinical application goals, optical or needle stroke length tolerances, electrical insulation barriers, and target retail packaging parameters.
Rapid CNC prototyping, precision mold building for ergonomic housing, custom silicone toolings, and PCB board circuit microcode programming.
Cleanroom cartridge packaging, ethylene oxide (EO) or gamma irradiation batch lot testing, followed by automated vacuum integrity verification.
Observed multi-week clinical results across verified aesthetic platforms including high-frequency micro-needling and phototherapy combinations.
*Representative clinical outcome demonstrating reduction in rolling acne scarring and dermal pore expansion following 4 sessions of automated transdermal micro-puncturing combined with 830nm near-infrared therapy.
Independently audited test reports and safety documentation to expedite Singapore HSA and regional ASEAN customs declarations.
CERT · 01 (EMC Compliance)
CERT · 02 (LVD Low Voltage)
CERT · 03 (RoHS Green Audit)
CERT · 04 (TUV/SGS Skin Test)
CERT · 05 (ISO Cleanroom Safety)
Anticipating the convergence of micro-electroporation, biodegradable micro-projections, and intelligent pressure-feedback actuators.
Next-generation derma devices are phasing into dual-action modalities where physical micro-channels receive localized electrical field electroporation, enhancing transdermal absorption rates of high-dalton hyaluronic acid molecules by over 400%.
Parallel to motorized pens, our factory cleanroom research explores crystallised lyophilized hyaluronic acid and peptide tips that dissolve directly inside the stratum corneum, creating a painless clinical alternative for home aesthetic maintenance regimens.
Our intelligent aesthetic platform roadmap integrates dynamic resistance capacitance sensors to read epidermal thickness variation across facial regions (forehead vs. peri-orbital tissue), automatically modulating stroke power to protect delicate structures.
Examine our full lineup of patented light therapy systems, laser caps, and precision microneedling derma pens manufactured directly from our Shenzhen production base.
Flexible medical silicone housing equipped with integrated cold compression functionality for professional post-peel recovery.
Ergonomic multi-spectrum photodynamic equipment calibrated to address complex skin blemish and rejuvenation requirements.
Low-level 650nm laser beam matrix engineered specifically to combat androgenetic alopecia and stimulate thinning hair follicles.
Contour-adaptive deep 630nm/830nm photodynamic device structured for high-throughput spa and aesthetic center installations.
Precision speed control micro-motor system paired with anti-backflow sterile cartridge assemblies for clinical transdermal delivery.
High-durability facial silicone and rigid structures featuring customizable wavelength combinations for global brand owners.
Wearable low-level light therapy system designed for home-use maintenance programs and clinical hair-thickening treatment lines.
Conformal fit engineering optimized for high spectral purity, ensuring maximized photon delivery to targeted dermal fibroblasts.
Everything procurement leads and aesthetic business owners need to understand regarding importation, factory verification, and custom manufacturing.
In Singapore, microneedling equipment can be categorized as a Class B or Class C medical device under the Health Sciences Authority (HSA) Medical Device Guidance depending on invasive depth and motorized penetration claims. Importers require a valid Dealer’s Licence (Wholesaler/Importer) and must submit compliance files including CE certification, ISO 13485 declarations, and biocompatibility test reports. Fanrun provides complete technical document dossiers to streamline your Singapore HSA medical device registration.
Yes. Fanrun provides end-to-end OEM private label solutions (custom silkscreen logo, body colorway anodization, bespoke aesthetic packaging, instruction manuals) and comprehensive ODM development (industrial casing tooling, custom PCB circuitry, specific LED wavelength selection, timer software, and mobile Bluetooth app integration).
Our complete product lines are CE (LVD, EMC) and RoHS certified. Skin-contact elements—including silicone light masks and microneedle cartridge assemblies—are fabricated with food-grade materials that have successfully cleared independent TUV and SGS testing audits.
Every single cartridge utilizes an integrated backflow silicone membrane barrier that seals the reciprocating drive needle shaft from fluids. Even when performing deep micro-needling with high fluid volumes (e.g., serum or PRF/PRP), liquids cannot traverse back into the handpiece, preventing patient-to-patient cross-contamination.
MOQ scales based on custom engineering depth. Standard laser engraving and branded unboxing for existing platforms begins at modest quantities of 100 to 300 units. Bespoke custom tooling, housing modifications, and complex software-integrated ODM projects generally scale from 500 to 1,000 units depending on mechanical specifications.
Whether launching an exclusive aesthetic line across Singapore medical clinics or expanding high-margin derma retail distribution across ASEAN, leverage our decadelong manufacturing authority.
To verify authenticity, request the certificate number from our team and check it on the issuing body's official portal. Contact us
