510(k) Report

FDA applicant

Canadian Pioneer Medical Technology Corporation (Cpmt Laser)

Vaugham, CA2 decisions2022–20220 recalls

FDA records 2 decisions for Canadian Pioneer Medical Technology Corporation (Cpmt Laser) (Vaugham, CA) in 2022: 2 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Canadian Pioneer Medical Technology Corporation (Cpmt Laser)’s devices, and how often a recall has named them.

FDA decisions per year

2in 2022

2022: 2
2022high 2 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Canadian Pioneer Medical Technology Corporation (Cpmt Laser) by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GEXPowered Laser Surgical Instrument2decisions

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K222673Alexandrite and Nd:YAG Laser models CANLASE and TORLASECanadian Pioneer Medical Technology Corporation (Cpmt Laser) · 2022
  • K222915Quadruple Laser System , Models : CPMT ARES , CPMT NEMESIS , CPMT NYX PLUS , CPMT GRACE PLUSCanadian Pioneer Medical Technology Corporation (Cpmt Laser) · 2022

All 2 as Canadian Pioneer Medical Technology Corporation (Cpmt Laser) →