KN-7000A PDT LED Light Therapy Machine for Skin Rejuvenation and Acne Care

Professional Multi-Wavelength LED Light Therapy for Aesthetic and Dermatology Use

Available across all EU countries except Germany

The KN-7000A is a professional LED photodynamic therapy (PDT) system developed for non-invasive skin treatment in clinical and aesthetic settings. Built around a 1,820-LED point matrix light source with multiple selectable wavelength combinations and an adjustable treatment head, it is positioned for institutions running acne care, skin rejuvenation, and inflammation-related treatment protocols.

Certification : FDA 510K cleared, CE MDR

Indications

The KN-7000A is positioned for:

• Inflammatory acne treatment
• Inflammation elimination
• Promotion of skin wound healing

Additional applications referenced for the platform include skin rejuvenation support and broader professional light-based skin care. Treatment selection and protocol should be determined by the treating practitioner based on the patient's condition.

Light Source

1,820 High-Power LEDs The treatment head uses 1,820 high-power LEDs arranged in a point matrix for even light distribution across the treatment area, offering higher output density than smaller single-panel LED systems.

Multiple Wavelength Combinations The system supports single-color and combined-color output across five base wavelengths — red, blue, yellow, green, and infrared — with the following combination options available:

• Red + Blue
• Red + Yellow
• Blue + Yellow
• Red + Infrared
• Yellow + Infrared

This gives practitioners the ability to tailor sessions to a specific skin concern, or combine wavelengths within a single treatment where the protocol calls for it.

Wavelength Reference

Key Features

Extendable, Adjustable Treatment Head The treatment head can be stretched and adjusted to suit different treatment areas, with a special electrical connection between the head and the base unit designed for faster, more convenient assembly.

Free-Designed Cantilever A cantilever mount allows the light source to be fixed and held at any angle or position, supporting flexible positioning across different treatment setups.

8" Rotating Touch Screen An 8-inch touch screen with rotation is built in for simple, straightforward operation, with 5 built-in common treatment plans for quick setup.

Continuous or Pulsed Irradiation The system supports both continuous and pulsed irradiation modes, giving practitioners flexibility to match delivery to the treatment protocol.

Adjustable Light Intensity Light source intensity can be adjusted according to different clinical needs, rather than being fixed at a single output level.

Voice Prompts Built-in voice prompts are designed to make the treatment experience more comfortable and reassuring for patients.

Dual-Layer Access Protection A dual switch key combined with password protection is built in to prevent the machine from being used by unauthorized or unrelated persons.

Non-Invasive, No Special Aftercare Treatment is non-invasive and non-damaging, with no reported side effects and no special aftercare required — patients can resume normal activity, including makeup application, immediately after a session.

Technical Specifications

Who It's For

• Dermatology clinics
• Medical aesthetics practices
• Skin treatment centers
• Hospital outpatient departments
• Professional beauty and skin care institutions

Why Choose the KN-7000A

The KN-7000A is built for institutions that want a versatile, single-platform PDT system rather than separate devices per wavelength. With five base colors, five combination modes, a high-density 1,820-LED matrix, adjustable treatment head, and straightforward touch-screen operation, it offers practical, structured light therapy across a broader indication range — from acne and inflammation to rejuvenation-focused protocols — in one unit.

Frequently Asked Questions

What is the KN-7000A used for? Professional light-based skin treatment, including inflammatory acne treatment, inflammation elimination, and promotion of skin wound healing, with the platform also supporting skin rejuvenation-focused protocols.

How many light color options does it offer? Five base colors — red, blue, yellow, green, infrared — plus five combination modes (e.g., red+blue, red+infrared).

How many LEDs does the treatment head use? 1,820 high-power LEDs in a point matrix arrangement.

Does it support different irradiation modes? Yes — both continuous and pulsed irradiation are supported.

Is aftercare required following treatment? No special aftercare is required; treatment is non-invasive and patients can resume normal skincare routines immediately.

ONE (1) YEAR LIMITED DEPOT WARRANTY (EU/EEA — CE MDR Version)

1. Warranty Provider and Term

This warranty is provided and administered strictly by the manufacturer of this particular product, not by Medaza Europe, d.o.o. The manufacturer warrants to the original purchasing entity ("Buyer") — including hospitals, clinics, and other licensed medical institutions within the European Union / European Economic Area — that the hardware product sold shall be free from defects in materials and workmanship under normal clinical use for a period of one (1) year from the date of shipment. This warranty is provided in addition to, and does not affect, any statutory rights the Buyer may hold as a matter of applicable EU or national consumer or commercial law.

2. Depot-Only Return Procedure

Warranty service is strictly a depot-return process conducted directly by the manufacturer of this particular product.

• First Step (Intake): To initiate a warranty claim, the Buyer must not contact the manufacturer directly. The Buyer must first contact Medaza Europe, d.o.o. by email at contacteurope2@medaza-platform.com.
• Delegation: Upon receipt of the email, Medaza Europe, d.o.o. — acting in its capacity as distributor under Regulation (EU) 2017/745 (the Medical Device Regulation, "MDR") — will delegate and coordinate the direct connection between the manufacturer (or the manufacturer's designated EU importer of record) and the Buyer, facilitating return logistics and securing the required Return Merchandise Authorization (RMA) number.
• Shipment: No shipments will be accepted by the manufacturer's facility without an active, authorized RMA number. The product must be securely packaged in its original packaging (or equivalent protective packaging), with all patient-identifying information removed or de-identified in accordance with Regulation (EU) 2016/679 (the General Data Protection Regulation, "GDPR") and applicable national data protection requirements prior to shipment, and shipped directly to the designated service facility of the manufacturer.

3. Allocation of Shipping Costs (Two-Way Shipping)

The Buyer assumes full financial responsibility for all shipping logistics, packaging, handling fees, customs/tariffs, and insurance transit costs associated with the warranty claim. This includes:

• Inbound Shipping: The cost to safely transport the product from the Buyer's facility to the designated service location of the manufacturer.
• Outbound Shipping: The cost to return the repaired or replaced product from the manufacturer's facility back to the Buyer's designated location within the EU/EEA.

4. Field Safety Corrective Action & Systemic Defect Exception

The shipping cost allocation in Section 3 shall be waived solely in the event that the returned product is officially determined by the manufacturer, its EU importer of record, Medaza Europe, d.o.o., or an authorized regulatory body (e.g., a national Competent Authority such as JAZMP, or another EU/EEA Competent Authority) to be subject to a Field Safety Corrective Action (FSCA), Field Safety Notice, or a verified batch-wide Systemic Manufacturing Defect, in accordance with the vigilance and market surveillance requirements of MDR Articles 87–92. In such extraordinary circumstances, the manufacturer will cover standard two-way ground shipping costs.

5. Warranty Exclusions

This warranty does not cover:

• Disposable clinical consumables (including but not limited to needles, sutures, applicators, and single-use accessories) once packaging is opened.
• Damage caused by accident, abuse, liquid spills, improper sterilization or disinfection, neglect, patient misuse, or unauthorized modifications or repairs.
• Damage resulting from use outside the manufacturer's labeled indications, intended purpose, or instructions for use (IFU), as defined under MDR Article 2.
• Normal wear and tear, consumable component degradation (e.g., lamps, filters, probes), or cosmetic degradation that does not affect device function or safety.
• Any device on which the Unique Device Identifier (UDI), serial number, or product identification label has been removed, altered, or defaced.

6. Incident Reporting and Vigilance

Nothing in this warranty limits or replaces the Buyer's independent obligation, as a healthcare institution or professional user, to report serious incidents or field safety issues involving this product in accordance with MDR Article 87. Reports should be directed to the manufacturer, to the manufacturer's designated EU importer of record, to Medaza Europe, d.o.o. as distributor, and, where required, to the relevant national Competent Authority (e.g., JAZMP) and/or logged via EUDAMED once the relevant EUDAMED modules become mandatory. Medaza Europe, d.o.o. will cooperate with the manufacturer, the importer of record, and Competent Authorities on any resulting vigilance investigation, corrective action, or reporting obligation.

7. Distributor Obligations Notice

For this product, Medaza Europe, d.o.o. acts solely as distributor under MDR Article 14; a separate, designated importer of record — not Medaza Europe, d.o.o. — fulfills the importer obligations under MDR Article 13 for this manufacturer's products. As distributor, Medaza Europe, d.o.o. confirms it verifies that the device bears the required CE marking and UDI, that it is accompanied by the manufacturer's required documentation and, where applicable, the importer's required labeling, and that appropriate storage and transport conditions are maintained while the product is under its responsibility. This warranty does not alter or diminish those statutory obligations, nor does it impose importer obligations on Medaza Europe, d.o.o.