Verify the machine, not the branding

Health Canada reports a falsified medical-device licence. It tells clinics to compare permanent-label manufacturer, device and model identifiers with MDALL, consult the manufacturer if uncertain, and stop using and safely dispose of counterfeits.

MDALL supports searches by company, licence, device name or identifier. It covers licensed Class II–IV devices; Class I devices and investigational or special-access devices are not listed. Our article does not authenticate any individual machine.

For people who received treatment

The agency advises patients with health concerns after laser therapy—including immediate pain, redness or swelling—to consult a licensed healthcare professional.

Counterfeit identification includes confirmation from the genuine manufacturer, which has a commercial interest. Grade A reflects the advisory, not treatment efficacy. Sources checked September 19, 2026.

Open the source file

These links support the claims above. Source dates, disclosures and limits are documented in the article and source list.

  1. Health Canada — counterfeit laser advisory RA-82651 (opens in a new tab)September 18, 2026
  2. Health Canada — Medical Devices Active Licence Listing (MDALL) (opens in a new tab)July 26, 2024 page details