Health Canada–Licensed Laser Systems
Official licence records available for independent verification.
Oakville Head Office & Showroom
Product consultations and confirmed appointments in Ontario.
Canada-Wide Delivery & Support Coordination
Delivery, installation and equipment onboarding coordinated for approved purchases.
2-Year Limited Warranty + 5-Year Parts Availability*
*Subject to the applicable warranty policy, issued purchase documents and product-specific terms.
Built Around the Questions Professional Buyers Actually Ask.
A successful device implementation begins with clear information, documented scope and realistic planning. DioLaz structures the purchasing experience around four areas.
Regulatory Transparency
For current licensed systems, we identify the applicable Health Canada Medical Device Licence and provide access to the official record so buyers can verify the information independently.
Defined Configuration & Scope
The selected model, handpieces, included accessories, services, delivery scope and commercial terms are documented through the applicable quotation, invoice, packing list and agreements.
Coordinated Implementation
Clinic location, delivery access, treatment-room readiness, electrical requirements, installation timing and equipment onboarding are reviewed according to the selected system and approved purchase scope.
Support Continuity
Existing customers have defined pathways for operational questions, warranty requests, troubleshooting, service coordination, parts and approved refresher resources.
REGULATORY ACCOUNTABILITY
Verify the device—not just the marketing.
DioLaz Canada Inc. is the company named on the active Health Canada Medical Device Licence records for the current flagship laser systems listed below.
We provide direct access to the official records so clinic owners, medical professionals and procurement teams can independently review the licence information alongside the product page, current User Manual and issued model and configuration documents.
Regulatory status is an important part of responsible due diligence, but it is not the only consideration. Buyers should also review the intended use, selected model, supplied components, operator requirements, site readiness, training scope, warranty and commercial documentation before approving an order.
Diode Laser Therapy System
A triple-wavelength 755 / 808 / 1064 nm platform designed for professional hair-removal workflows, with adjustable treatment controls and integrated contact cooling.
Health Canada Medical Device Licence 114257
Fractional CO₂ Laser Therapy System
A 10,600 nm platform supporting professional fractional resurfacing and selected CO₂ workflows within the device’s intended use and the operator’s qualified scope.
Health Canada Medical Device Licence 114258
Picosecond Laser System
A dual-wavelength 1064 / 532 nm platform supporting professional tattoo-removal, benign-pigment and skin-rejuvenation workflows within the device’s intended use.
Health Canada Medical Device Licence 115451
PROFESSIONAL SYSTEMS
A Focused Portfolio for Professional Aesthetic Practices.
We focus on professional systems that can be clearly documented, implemented and supported—not an endless catalogue of unrelated equipment.
Explore the current DioLaz flagship laser portfolio by treatment category, workflow and implementation requirements.
Not Sure Which System Fits Your Practice?
Discuss your planned services, operator background, clinic location, treatment space, purchasing timeline and documentation requirements with a DioLaz Product Specialist.
THE PROCUREMENT JOURNEY
From initial comparison to ongoing support.
Every clinic has a different service model, team, facility and purchasing timeline. Our process is designed to identify those differences before the final order scope is confirmed.
Step 1
Define the Practice Need
Discuss the services you plan to introduce, your current equipment, operator background, province, target timeline, treatment-room constraints and operational priorities.
Step 2
Review the System & Documentation
Compare system capabilities, available configurations, included components, official licence information, product documentation, implementation requirements and applicable policies.
Step 3
Confirm the Commercial & Site Plan
Confirm the selected model, quotation, purchase structure, financing or program pathway, delivery access, electrical requirements and treatment-room readiness.
Step 4
Coordinate Delivery & Equipment Onboarding
Arrange receiving, installation, setup, basic equipment operation, cleaning, maintenance guidance and the training documentation included in the approved purchase scope.
Step 5
Continue with Defined Support
Use the appropriate DioLaz support channel for operational questions, warranty requests, technical troubleshooting, parts, service coordination and approved refresher resources.
Support should continue after the delivery date.
Device ownership continues after installation. Routine cleaning, preventive care, documentation, staff changes, service requests and parts planning all affect the long-term experience.
DioLaz publishes programs and policies so clinics can understand how support is accessed, what information may be required and which terms apply before and after a purchase.
The DioLaz Resource Centre currently includes master and product-specific warranty documents, equipment onboarding policies, shipping and delivery terms, return and cancellation information, education pricing, trade-in and buyback programs, authorized clinic partner resources and official contact pathways.
Eligibility, availability and final coverage are determined by the applicable policy and issued transaction documents.
PROFESSIONAL PRACTICES
Built for professional decision-makers.
DioLaz works with professional buyers evaluating equipment for a clinic, medical-aesthetic practice or qualified healthcare setting.
Our conversations commonly involve clinic owners, physicians, nurses, medical aestheticians, laser professionals, operations teams, procurement personnel and qualified entrepreneurs preparing to introduce a professional service line.
Professional Responsibility Note
Purchasing or owning a device does not determine who may perform a treatment.
Clinics and operators remain responsible for professional qualifications, independent clinical education, insurance, scope-of-practice requirements, client assessment, facility policies and all applicable provincial, local and professional obligations.
DioLaz equipment onboarding addresses the operation and care of the purchased system. It does not replace independent clinical education or professional qualification.
