
Handpiece front view
Review the contact window and handpiece form factor as part of a product demonstration.































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DioLaz Health Canada Licensed Hair Removal Laser Machine 3 Wavelengths
Review the equipment, handpiece interface and implementation requirements in one place. Built around 755 / 808 / 1064 nm delivery, adjustable output and sapphire contact cooling.

Licence holder / manufacturer: DioLaz Canada Inc. Review the official record for current status.

A purchasing overview for clinic owners, procurement teams and qualified operators—not a substitute for the User Manual or a configuration-specific quotation.
Compare wavelength delivery, fluence, repetition rate, pulse duration and cooling specifications against your clinic’s requirements.
Confirm the console, handpiece, accessories and services in the quotation. Gallery photos are not a packing list.
Review site readiness, operator training, service arrangements and applicable purchase policies before order approval.
Recent product-gallery views show the contact end and a touch-screen handpiece interface. Match the ordered handpiece to the selected configuration and quotation.

Review the contact window and handpiece form factor as part of a product demonstration.

The close-up shows the handpiece display. Values shown in the photograph are illustrative, not recommended treatment settings.
Model years and availability are controlled by the product selector and confirmed quotation. Different handpieces are not automatically included together.

Combined diode delivery at 755, 808 and 1064 nm, with SHR and HR workflows for professionally assessed treatment plans.
Continuous movement for broader treatment zones. Use must follow operator training and the applicable protocol.
Pulse placement for focused treatment zones. Parameter selection and technique must follow the User Manual.
Treatment suitability, including Fitzpatrick skin types I–VI, requires individual assessment. Published ranges are not a clinical protocol.
Match each function to its actual component, then confirm installation, compatibility and operator requirements with DioLaz.

Curved light-guide attachment for small or contoured areas. Confirm compatibility and included accessories for the ordered handpiece.

The brochure specifies sapphire-tip cooling down to approximately −32 °C. This is a tip specification—not a target skin temperature.

The rear interface is labelled for an interlocking device. Verify the treatment-room connection and safety checks during commissioning.
Additional gallery details support pre-installation discussions. Final supplied items and quantities must be listed in the quotation or packing list.

Confirm rear clearance, access and installation requirements for the supplied unit.

Follow the current User Manual for water specifications, inspection and maintenance intervals.

Confirm the supplied foot control, connection and intended use for your configuration.

Confirm included eyewear, wavelength coverage and protection specifications before clinical use.
Photos alone do not establish electrical requirements, eyewear certification, interlock commissioning or the complete scope of supply.
Reference data for your equipment comparison and procurement file. All four sections are expanded initially; each can still be collapsed individually.
Order confirmation: The selected model, handpiece, accessories, delivery, training, warranty and commercial terms must be confirmed in the quotation, order documents and applicable policies.
Regulator: Health Canada
Medical Device Licence: No. 114257
Device class: Class III
Licence type: System
Licence holder / manufacturer: DioLaz Canada Inc.
First issue date: 2025-10-31
Official licence name: DIODE LASER THERAPY SYSTEMS
Current status: Consult the live MDALL record
Wavelengths: 755 / 808 / 1064 nm
Peak optical output: Up to 1,200 W
Fluence: 1–100 J/cm²
Repetition rate: Up to 10 Hz
Treatment spot: 12 × 24 mm · 2.88 cm²
Pulse duration: 5–300 ms
Beam profile: Uniform top-hat
Sapphire-tip cooling: Down to approximately −32 °C
Reference values reflect the published DioLaz brochure. Confirm specifications for the ordered configuration. Optical output is not the electrical input rating. *Tip temperature is not a skin-temperature target; clinical settings must follow the User Manual.
Confirm training arrangements, qualified users and access to the current DioLaz User Manual before clinical use.
Document client assessment, treatment suitability, selected parameters and treatment endpoints in accordance with the applicable protocol.
Confirm room access, electrical requirements, interlock installation, emergency controls and local laser-safety procedures before commissioning.
Configuration: Selected console, model, handpiece and compatible accessories.
Supply & documentation: Included items, quantities, User Manual and configuration-specific technical information.
Implementation & support: Installation responsibilities, training arrangements, service contact and warranty terms.
Purchase route: Order placement, financing or trial eligibility, delivery and return conditions under the applicable policies.
Share your preferred configuration, clinic location and purchase timeline. Request a configuration-specific quotation and confirm the relevant programs and policies.
For professional use only. Review contraindications, precautions, safety requirements and treatment parameters in the DioLaz User Manual before clinical use.
If you have any questions, you are always welcome to contact us. We'll get back to you as soon as possible.
Shipping Information
At DioLaz Canada Inc., every order is handled with exceptional precision and care, ensuring your premium medical and aesthetic products reach you safely, securely, and promptly.
Customer Support
DioLaz Canada Inc. stands confidently behind the quality and reliability of our Medical and Aesthetic Devices. Our comprehensive warranty policy is carefully crafted to provide peace of mind to our valued customers.
Contact Us
customersupport@diolaz.com