Hongkong Sylustar Science And Technology Co., Ltd — Verified Supplier
About Hongkong Sylustar Science And Technology Co., Ltd - Skin Care Equipment Supplier in Hong Kong
Hong Kong‑based Hongkong Sylustar Science And Technology Co., Ltd operates as an imported supplier listed with five active products. The catalogue focuses on aesthetic medical devices used for skin treatment and rejuvenation. All items fall under the broader HS chapter 90 for optical and medical instruments, specifically the 9018 - 9019 range that covers laser and phototherapy equipment. The company’s product portfolio is marketed to clinics and distributors that require compliant laser or radio‑frequency systems. No additional product categories are listed beyond the five skin‑care focused systems.
The Mini‑IPL system delivers intense pulsed light across multiple wavelengths for hair removal and pigment reduction. The Nd:YAG Q‑Switched laser skin care system operates at 1064 nm with nanosecond pulses for tattoo and lesion removal. The CO₂ fractional laser system provides ablative resurfacing with columnar micro‑thermal zones. The RF (radio frequency) system offers non‑ablative tightening through controlled dermal heating. The LED skin rejuvenation system uses red and near‑infrared light for collagen stimulation and anti‑inflammatory effects.
Product Range and Specialties of Hongkong Sylustar Science And Technology Co., Ltd
The Mini‑IPL unit typically offers selectable wavelengths from 515 nm to 1064 nm, fluence up to 30 J/cm² and pulse widths between 1 ms and 100 ms, matching industry standards for hair‑removal and photorejuvenation. Nd:YAG Q‑Switched lasers are commonly specified with pulse energies of 0.5‑5 J and repetition rates of 1‑10 Hz, conforming to IEC 60601‑2‑22 safety limits for dermatological applications. CO₂ fractional lasers are graded by peak power (often 10‑30 W) and spot density (e.g., 100‑300 micro‑holes cm⁻²), a typical specification for resurfacing procedures. RF skin‑tightening devices are usually described by output power (10‑30 W) and operating frequency (0.5‑1 MHz), aligning with non‑ablative tightening protocols. LED rejuvenation systems are measured by irradiance (e.g., 30‑80 mW/cm²) and treatment time (10‑30 min), reflecting common clinical regimens. All five systems fall within the medical aesthetic equipment segment where CE marking, ISO 13485 quality management and, where applicable, FDA Class II clearance are standard regulatory expectations.
Trade and Export Information - Hongkong Sylustar Science And Technology Co., Ltd
Hong Kong functions as a major trans‑shipment hub for medical aesthetic equipment, allowing manufacturers to access global markets through sea and air logistics. Exporters of laser and phototherapy devices from the region typically ship using 20‑foot or 40‑foot containers with protective foam padding, or via air freight for faster delivery to Europe, the Middle East, Southeast Asia and North America. HS code 9018 covers laser apparatus and related equipment, while HS code 9019 applies to other medical instruments; customs authorities in importing countries often request a Certificate of Origin and a Declaration of Conformity for these codes. Buyers usually require CE certificates confirming compliance with the Medical Device Regulation (MDR) and, for certain markets, ISO 13485 certification to verify the supplier’s quality system. In addition, many importers request test reports for optical output, electromagnetic compatibility (EMC) and laser safety class (e.g., Class IIIb or IV) before clearance.
Sourcing from Hongkong Sylustar Science And Technology Co., Ltd - Buyer Guidance
When sourcing from Hongkong Sylustar, buyers should request the full technical data sheet for each system, including wavelength range, pulse energy, power output, treatment spot size and safety standards compliance. Verify that the supplier can provide a current CE Declaration of Conformity, ISO 13485 certificate and, if required by the destination market, FDA or other national registration documents. Request independent test reports for laser output stability, RF power consistency and LED irradiance, and confirm packaging details such as double‑wall wooden crates or reinforced pallets for sea freight. Confirm the minimum order quantity, lead time for production and any pre‑shipment inspection that aligns with the buyer’s compliance program.
Frequently Asked Questions About Hongkong Sylustar Science And Technology Co., Ltd
What types of skin‑care devices does Hongkong Sylustar list in its catalogue?
The catalogue includes a Mini‑IPL system, an Nd:YAG Q‑Switched laser skin care system, a CO₂ fractional laser system, an RF (radio frequency) skin‑tightening system and an LED skin rejuvenation system.
Which HS codes are relevant for these devices?
The devices fall under HS chapter 90, specifically HS code 9018 for laser apparatus and HS code 9019 for other medical instruments such as RF and LED treatment units.
What safety or quality certifications should a buyer request?
Buyers should ask for CE marking documents, an ISO 13485 quality‑management certificate, and, where applicable, test reports that demonstrate compliance with IEC 60601‑2‑22 for laser safety.
What typical specifications are used to evaluate the Mini‑IPL system?
Evaluations focus on selectable wavelength range (usually 515‑1064 nm), fluence levels up to 30 J/cm², pulse duration (1‑100 ms) and built‑in cooling mechanisms to meet skin‑safety standards.
Are sample units or trial runs available before a full order?
Suppliers of medical aesthetic equipment commonly provide a limited number of demo units or arrange on‑site trials, but the buyer must confirm availability and any associated shipping or insurance costs in advance.
What are the usual packaging and shipping methods for these systems?
Products are typically packed in reinforced wooden crates with foam inserts, shipped in 20‑foot or 40‑foot containers for sea freight, or via air freight in climate‑controlled pallets for faster delivery.
What is a typical lead time for an order from Hongkong Sylustar?
Lead times generally range from 4 to 8 weeks after receipt of a confirmed purchase order, depending on the specific device configuration and any required certification documentation.
Which regions normally import aesthetic laser and RF equipment from Hong Kong?
Key import regions include East and Southeast Asia, the Middle East, Europe and North America, where clinics and distributors seek CE‑marked or FDA‑registered medical aesthetic devices.






