Clinic Device Consultation

Professional equipment inquiries for Canadian clinics
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DioLaz Canada · B2B clinic solutions

Plan your next professional device with confidence.

Compare professional medical and aesthetic platforms, review Health Canada licence information, and plan configuration, financing, delivery, installation and equipment onboarding with a DioLaz Product Specialist.

This page is for professional equipment procurement. DioLaz does not book patient treatments through this form.
Regulatory transparency Product-specific licence information and official verification links.
Canada-wide coordination Delivery, installation and site-readiness planning for approved purchases.
Equipment onboarding Setup, interface, handpiece, cleaning and maintenance orientation.
Long-term support Two-year limited warranty and five-year parts availability under policy terms.
Professional platforms

Start with the service line your clinic is planning.

Review the clinical workflow, operator requirements, room considerations and commercial scope—not only the headline specifications.

Hair removal Class III · MDL 114257

Triple-WavelengthDiode Laser

For clinics evaluating a dedicated professional hair-removal platform with large-area coverage and configurable handpiece workflows.

  • 755 / 808 / 1064 nm wavelength platform
  • 12 × 24 mm treatment spot and up to 10 Hz
  • Traditional or built-in touchscreen handpiece configurations
Skin resurfacing Class III · MDL 114258

Fractional CO₂Laser

For appropriately qualified clinics comparing fractional resurfacing, focused delivery and specialty-probe workflows in one configurable platform.

  • 10,600 nm carbon dioxide laser platform
  • Up to 40 W adjustable output and articulated beam delivery
  • Model, handpiece, probes and accessories confirmed before order
Tattoo & pigment Class III · MDL 115451

PicosecondLaser

For clinics building professional tattoo-removal, benign-pigment and non-ablative skin-rejuvenation workflows around a true picosecond platform.

  • 1064 / 532 nm dual-wavelength delivery
  • Approximately 450 ps pulse duration and up to 10 Hz
  • 2–10 mm continuous spot-size control
A B2B procurement conversation

Evaluate the purchase around your clinic—not around a generic sales script.

A Product Specialist can help organize the commercial and implementation questions that should be clear before an order is approved.

01

Service goals

Which professional service category, client population and workflow are you planning to add?

02

Operator readiness

Who will operate the device, and what clinical education, licensing and safety requirements apply?

03

Site readiness

Room access, electrical planning, delivery path, ventilation and treatment-room setup.

04

Commercial structure

Configuration, included accessories, financing pathway, implementation timing and written terms.

Verify before you buy

Verify each product-specific licence record before purchase.

Open the regulator’s current record and confirm the device name, class, licence holder and included models—not only a broad “medical grade” claim.

Health Canada MDL 115451

Picosecond LaserSystem

Active Class III device-family licence listed under DioLaz Canada Inc.

Open official MDALL record ↗
Licence status, intended use and included models are product-specific and should be verified against the current Health Canada record and DioLaz product documentation. The regulatory address shown in an official record may differ from the current Oakville showroom address.
From evaluation to implementation

Know what happens before and after purchase.

The issued quotation, invoice, signed agreement and applicable policies control the final configuration, services and commercial terms.

01

Consultation

Review service goals, device fit, timeline and initial purchasing questions.

02

Written scope

Confirm model, handpieces, accessories, pricing, payment structure and policies.

03

Site planning

Coordinate delivery access, treatment-room readiness and installation scheduling.

04

Installation & onboarding

Equipment setup, interface, handpiece handling, cleaning and routine maintenance orientation.

05

Ongoing support

Technical assistance, warranty process, parts coordination and approved follow-up support.

DioLaz equipment onboarding is not clinical education, medical advice, scope-of-practice authorization or live-patient treatment training. Operators remain responsible for appropriate professional qualifications, independent clinical education, local requirements and patient-specific decisions.
Purchase pathways and resources

Review the options that may apply to your clinic.

Availability and eligibility are approval-based. The applicable written policy and signed transaction documents always control.

In-House Financing

Review the approval-based initial payment, tax, term, APR, payment and documentation requirements.

Read financing policy →

5-Day In-Clinic Trial

Available for approved Diode and Fractional CO₂ evaluations in the GTA and GVA, subject to deposit, logistics and signed-program terms.

Review trial program →

Programs, Policies & Support

Access education, trade-in, buyback, warranty, training, shipping, returns, FAQ and contact resources.

Open resource centre →
Product consultation

Tell us what your clinic is planning.

Fields marked with an asterisk are required. Do not submit payment-card details, patient records or unnecessary sensitive personal information.

Thank you. Your consultation request has been submitted.

A DioLaz team member will review the business, device and timeline information you provided and follow up using your preferred contact method.

Before you inquire

Common procurement questions.

For product-specific terms, consult the current product page, formal policy and written transaction documents.

What should a clinic evaluate before selecting a device platform?

A structured review should consider the services being added, licensed intended use, operator qualifications, treatment-room and electrical requirements, expected workflow, financing, warranty, parts availability and implementation support. DioLaz can help organize the procurement review; clinical suitability and treatment decisions remain with qualified professionals.

Are DioLaz laser platforms licensed by Health Canada?

Licence status is product-specific. The DioLaz Diode Laser, Fractional CO₂ Laser and Picosecond Laser pages identify active Class III Medical Device Licence records 114257, 114258 and 115451. Use the official links above to verify the current records.

What does equipment onboarding include?

Depending on the device and written order scope, onboarding can cover setup and shutdown, interface navigation, handpiece or probe handling, cleaning, routine maintenance and safety functions. It does not replace clinical education or authorize live-patient treatment.

Can I discuss financing or an in-clinic trial?

Yes. Financing is approval-based. The current in-clinic trial program applies only to eligible Diode and Fractional CO₂ evaluations in the Greater Toronto Area and Greater Vancouver Area, with deposit, logistics and signed-program requirements. Review the linked policies before relying on availability.

Can I visit the Oakville showroom?

Yes, after receiving written confirmation of an appointment. The head office and showroom is located at Unit 5, 785 Pacific Road, Oakville, Ontario L6L 6M3. Unconfirmed walk-ins and unscheduled demonstrations are not accepted.

Move your clinic’s equipment plan forward with a structured consultation.

Share your business, province, platform of interest and expected timeline. A DioLaz Product Specialist will review the request and coordinate the appropriate next step.