About Beijing JKX-Group Company - Cosmetics & Beauty Parlour Equipments Supplier in China

China is the origin of Beijing JKX-Group Company, which currently lists 14 active products on the platform. The catalogue focuses on aesthetic and medical equipment used in beauty salons and clinics, covering IPL hair‑removal devices, diode laser hair‑removal systems, and HIFU (High‑Intensity Focused Ultrasound) machines for skin tightening and body slimming. All IPL‑related items fall under HS chapter 85, code 8543.70, which classifies electronic apparatus for medical use, while the diode laser and HIFU units are coded 9018.90, covering surgical, dental or medical instruments. The listed products specify housing materials such as ABS plastic, stainless steel, aluminum alloy, and incorporate components like sapphire crystal, LED/Flash lamps, GaAlAs semiconductor diodes, and medical‑grade optical fibers. The supplier’s top categories are recorded as Cosmetics & Beauty Parlour Equipments, Agriculture and Other Medical Equipments.

The product titles include variations of IPL devices for hair removal and skin rejuvenation, several 808 nm diode laser machines promising up to 20 million shots, and multiple HIFU machines with four‑head configurations for face and body treatments. Materials range from ABS plastic housings with sapphire crystal windows to stainless‑steel frames combined with optical‑grade glass or German‑sourced diode modules. HS codes 8543.70 and 9018.90 appear repeatedly, indicating that the majority of the catalogue belongs to electronic medical apparatus and surgical instrument categories. No additional product categories beyond the three listed are present in the data. The information is limited to the catalogue entries without any claim of certifications or export volumes.

Product Range and Specialties of Beijing JKX-Group Company

The catalogue offers four IPL‑type devices, each built on ABS plastic housings with sapphire crystal or LED/Flash lamp modules, and classified under HS 8543.70. In the broader industry, IPL systems typically operate in the 600‑1000 nm wavelength range, deliver pulse energies of 5‑30 J/cm², and are evaluated against IEC 60601‑2‑57 safety standards. Diode laser hair‑removal machines in the list are 808 nm devices with stainless‑steel or aluminum alloy housings, placed under HS 9018.90. Industry practice expects output powers between 10‑30 W, pulse repetition rates of 1‑10 Hz, and a shot guarantee often expressed as 10‑20 million pulses. HIFU machines for facial and body applications also fall under HS 9018.90 and usually feature medical‑grade ABS or stainless‑steel housings, transducers operating at 1‑3 MHz frequency, focal depths of 1‑3 cm, and power outputs of 2‑5 kW per head. Typical certifications for these categories include CE marking, ISO 13485 quality management, and, for markets like the United States, FDA 510(k) clearance. Buyers often request material safety data sheets for plastics, laser safety certificates, and performance test reports that confirm fluence, focal accuracy and thermal dosing.

Trade and Export Information - Beijing JKX-Group Company

China is a major exporter of aesthetic medical equipment, and shipments of IPL, diode laser and HIFU devices are routinely directed to Southeast Asian beauty markets, the Middle East, European Union member states and North‑American clinics. HS chapter 85 (code 8543.70) and chapter 90 (code 9018.90) are monitored by customs authorities for compliance with safety standards such as IEC 60601‑2‑57 for IPL and IEC 60825 for laser products. Importers commonly require CE conformity, ISO 13485 certification, and test reports from accredited labs before granting market entry. Logistics for the 14‑item range typically involve containerized shipping, with bulkier HIFU units packed in wooden crates or reinforced cardboard, fitting a standard 20‑ft container (approximately 30‑35 m³) or a 40‑ft container for larger orders. Freight terms such as CIF or FOB are standard, and Chinese exporters often provide pre‑shipment inspection certificates to satisfy buyer‑side quality assurance.

Regulatory expectations differ by destination: EU buyers look for EU Declaration of Conformity and a Notified Body report, while Gulf Cooperation Council (GCC) importers may request GCC‑S certification in addition to CE. In the United States, FDA 510(k) clearance is mandatory for laser and HIFU devices marketed as medical equipment. Chinese manufacturers typically label each unit with model number, voltage rating, and safety warnings in both English and Chinese, and they may offer after‑sales service contracts that align with international warranty norms.

Sourcing from Beijing JKX-Group Company - Buyer Guidance

When sourcing from Beijing JKX-Group Company, buyers should request the latest CE test report, ISO 13485 certificate and, where applicable, FDA 510(k) documentation for diode laser and HIFU units. Verify that the IPL devices meet IEC 60601‑2‑57 safety limits and that laser output power, wavelength and shot count are confirmed by an independent laser safety audit. Request a detailed specification sheet that lists housing material grades (e.g., ABS grade PC‑ABS, stainless‑steel 304), component suppliers, electrical ratings and warranty terms before confirming an order.

Typical minimum order quantities for aesthetic devices range from one unit for sample evaluation to 10‑20 units for bulk purchase, with lead times of 30‑45 days after receipt of a confirmed purchase order and required pre‑shipment inspection. Buyers should also confirm packaging dimensions, weight per carton and whether the supplier can provide individual unit serial numbers for traceability. Ensuring that the supplier can furnish a pre‑shipment inspection certificate (e.g., SGS, BV) and a full packing list aligned with HS codes 8543.70 and 9018.90 will reduce customs delays.

What types of aesthetic equipment does Beijing JKX-Group Company list?

The supplier lists IPL hair‑removal and skin‑rejuvenation devices, 808 nm diode laser hair‑removal machines, and HIFU machines for facial tightening and body slimming, all classified under HS 8543.70 or 9018.90.

Which HS codes are associated with the products?

IPL‑related devices use HS code 8543.70, while diode laser and HIFU machines are recorded under HS code 9018.90, both falling under medical‑electronic and surgical instrument categories.

What materials are used in the housings of these devices?

The catalogue specifies ABS plastic, stainless steel, aluminum alloy, and medical‑grade ABS combined with sapphire crystal or optical‑grade glass for windows and lenses.

What certifications should a buyer request before purchasing?

Buyers should ask for CE conformity reports, ISO 13485 quality‑management certificates, and, for U.S. market entry, FDA 510(k) clearance; laser safety certificates (IEC 60825) are also advisable.

What are typical minimum order quantities and lead times?

Sample orders can start at a single unit, while bulk purchases usually require 10‑20 units. Standard lead time after order confirmation is 30‑45 days, depending on production scheduling and inspection requirements.

How are the devices typically packaged for export?

Bulkier HIFU units are packed in reinforced wooden crates or sturdy cardboard, fitting standard 20‑ft or 40‑ft containers; smaller IPL and laser devices are usually boxed in individual cartons with protective foam inserts.

What documentation is needed for customs clearance?

A commercial invoice listing the correct HS code, a packing list, the supplier’s CE declaration (or other required regional certificates), and a pre‑shipment inspection certificate are standard documents for customs clearance.

Can buyers request sample units for testing?

Yes, buyers can request a single unit sample; the supplier typically provides a quotation that includes sample cost, shipping terms (often CIF) and expected delivery time.