Explore our certified flagship innovations spanning picosecond optics, radiofrequency, and diode laser platforms.
A definitive guide for global brand owners, medical equipment distributors, and aesthetic clinic chains seeking high-yield OEM/ODM manufacturing partnerships.
Delivering sub-nanosecond pulse widths (375ps to 600ps) to induce photoacoustic shockwaves, fracturing target chromophores into microscopic dust without collateral thermal necrosis.
Generating Laser-Induced Optical Breakdown (LIOB) in the dermis to trigger localized wound-healing cascades, neocollagenesis, and elastin fiber reorganization for non-invasive skin remodeling.
Manufactured under ISO 13485 quality frameworks, utilizing imported dual-pump laser cavities, sealed optical paths, and 7-joint articulated transmission arms for steady energy fluency.
Understanding why true picosecond pulse duration delivers superior safety profiles and clinical efficacy compared to legacy nanosecond Q-switched lasers.
Traditional laser facial treatments rely predominantly on photothermal breakdown, wherein target pigment granules absorb optical energy, convert it into heat, and thermally expand to disintegrate. However, if the pulse duration exceeds the thermal relaxation time of the target, excess thermal energy radiates into surrounding healthy tissue, leading to erythema, post-inflammatory hyperpigmentation (PIH), or scarring—especially in Fitzpatick skin types IV-VI.
In contrast, Pico Laser Face technology operates under the principle of Stress Confinement. By delivering giant peak power pulses within picoseconds (trillionths of a second), energy is delivered faster than the acoustic expansion time of melanin granules. This creates an intense photoacoustic pressure wave, causing mechanical fragmentation of pigment into dust-like micro-particles that are swiftly phagocytized by the lymphatic system.
| Performance Feature | Legacy Nanosecond Q-Switched Laser | Advanced OEM Pico Laser Platform |
|---|---|---|
| Primary Mechanism | Photothermal (Heat accumulation) | Photomechanical / Photoacoustic Shockwave |
| Target Particle Fragmentation | Coarse pebble-like fragments | Ultra-fine dust-like particles |
| Dermal Rejuvenation Mechanism | Thermal micro-injuries | Laser-Induced Optical Breakdown (LIOB) |
| Risk of PIH (Darker Skin Types) | Moderate to High risk | Extremely Low risk |
| Required Clinical Sessions | 8 to 12 sessions | 3 to 5 sessions |
| Patient Downtime | 3 to 7 days erythema/edema | 2 to 12 hours micro-flushing |
Mining user intent across clinical dermatological centers, commercial MedSpas, and mobile aesthetic franchises.
Traditional thermal lasers frequently trigger rebound melasma. Picosecond 1064nm low-fluence toning breaks down dermal melanophages without activating melanocytes, offering a safe long-term suppression protocol.
Utilizing micro-lens arrays (MLA) or diffractive lens arrays (DLA), pico lasers create localized plasma vacuoles in the epidermis and upper dermis (LIOB), stimulating collagen type I & III production while keeping the stratum corneum intact.
Combination protocols incorporating nano-carbon suspension lotions with 1064nm quasi-long pulse modes deep-cleanse sebaceous glands, shrink enlarged facial pores, and optimize skin texture in high-volume commercial salons.
Leveraging high-tech ecosystem integration, precision optical cleanrooms, and cost-efficient scalable assembly.
Founded in Beijing, China, Beijing UNT Technology Co., Ltd. has established itself as a premier high-tech enterprise occupying over 6,000 square meters of state-of-the-art administrative and manufacturing floor space, housing a dedicated 100 m² clean room.
Our OEM/ODM manufacturing capability spans the complete engineering spectrum: from in-house PCB electronic hardware design and laser optical cavity machining to UI/UX Android OS software development and housing ergonomics prototyping.
Continuous innovation in non-invasive and minimally invasive laser technologies tailored for dynamic skin phenotypes.
Streamlined assembly protocols following ISO 13485 frameworks to optimize throughput and eliminate component waste.
Rigid quality gates verifying focal spot uniformity, laser rod pumping efficiency, and harmonic crystal conversion.
Partnerships with DHL, FedEx, TNT, UPS, and EMS guarantee 3-5 days expedited worldwide door-to-door delivery.
Architecting customized hardware, intelligent software interfaces, and brand identity solutions for enterprise procurement.
Custom chassis molding, metallic finish selection, multi-articulated arm housing choices, and branded handpiece ergonomics designed to reflect your brand's unique market identity.
Integration of UNT's proprietary SmartDepi Android System. Software customization includes custom boot logos, localized language support, client database storage, and cloud telemetry.
Customizing optical cavities, single vs. double rod configurations, xenon flashlamp durability up to 10 million shots, and modular plug-and-play internal component architecture.
Evaluating vendor capability, after-sales technical infrastructure, and international compliance guarantees.
Medical equipment compliance is paramount. UNT machines possess FDA 510(k) clearances, MDR CE certifications, TGA compliance, and ISO 13485:2016 certification (MDSAP based), facilitating smooth customs clearance across North America, Europe, Latin America, and Asia-Pacific.
To eliminate post-sale friction for Western buyers, UNT maintains a dedicated European Customer Service Center—"APEX"—in the Netherlands. Services include hands-on machine experience, local technical training, spare parts distribution, and rapid door-to-door field maintenance across Europe.
All OEM laser systems come backed by a comprehensive 2-year warranty and lifetime maintenance support. Our 24/7 engineering helpdesk ensures zero clinic downtime through remote diagnostic software and immediate modular part dispatch.
A corporate timeline of innovation, global expansion, and medical certification milestones.
UNT was established in Beijing and Hong Kong, focusing on high-end medical aesthetic technology R&D.
Independently engineered and commercialized advanced intense pulsed light (IPL) treatment platforms.
Pioneered the touch-screen interactive operation handle for diode laser equipment, setting a new industry standard.
Launched complete lines of Q-switched, Picosecond, and Nd:YAG laser systems worldwide.
Introduced the world's first Android operating system dedicated to medical laser parameter control.
Expanded manufacturing headquarters to 6,000 square meters in Beijing with over 130 specialized employees.
Secured four major FDA 510(k) clearances covering Diode Lasers, MuseShape, Nd:YAG, and Cryo Slimming devices.
Achieved ISO 13485 (MDR) and MDSAP certifications, while launching the APEX Netherlands service center.
Ensuring absolute structural integrity, optical path alignment, and system longevity.
Prototypes are modeled using specialized CAD/CAM tools, followed by 3D optical path simulation to optimize handle balance and laser delivery efficiency.
Laser optical crystals, mirrors, and cavity housings are assembled in ISO Class 7 dust-free cleanrooms to prevent optical contamination and beam distortion.
Every system undergoes 48 hours of continuous full-fluence firing tests and thermal stability monitoring prior to final quality assurance sign-off.
Unique Serial Numbers (SN) are laser-etched onto internal components, allowing complete lifetime tracking from raw material batches to clinical end-users.
Addressing essential technical, commercial, and clinical queries from distributors and medical equipment buyers.
A: True picosecond machines deliver pulse durations strictly below 1 nanosecond (typically 375ps–600ps), generating strong photoacoustic pressure. Pseudo-picosecond devices often utilize nanosecond Q-switched circuits with stretched pulses (2ns–5ns), relying primarily on photothermal heat which increases PIH risk on sensitive skin types.
A: We provide comprehensive end-to-end customization including industrial casing geometry, custom colorways, brand logo silk-screening, handpiece optic configurations, localized touch screen GUI, Android SmartDepi integration, and custom software protocol presets.
A: We supply full technical documentation packages including ISO 13485 audit reports, CE MDR certification compliance dossiers, IEC 60601-1 electrical safety test reports, and FDA 510(k) master file references to streamline local ministry of health registrations.
A: Standard OEM sample builds require 7–14 working days. Bulk production orders (50+ units) are fulfilled within 20–30 days. Delivery via express air logistics (DHL, FedEx, UPS) takes 3 to 5 business days globally.
A: UNT integrates premium imported UK-made xenon lamps housed within high-reflectivity cavity chambers, rating the handpiece for up to 10 million shots with minimal energy decay over its lifecycle.
A: APEX provides European clients with local equipment demonstrations, hands-on clinical operator training, immediate spare parts dispatch, and door-to-door repair services within the EU without international customs delays.
Expand your clinic portfolio with certified body contouring, multi-wavelength diode hair removal, and tattoo removal devices.
UNT TECH
