510(k) Report

FDA applicant

Cpmt Laser (Canadian Pioneer Medical Technology Corporation)

Toronto, CA2 decisions2024–20250 recalls

FDA records 2 decisions for Cpmt Laser (Canadian Pioneer Medical Technology Corporation) (Toronto, CA) from 2024 to 2025: 2 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and NGX (Stimulator, Muscle, Powered, For Muscle…). Its devices cite 2 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 Cpmt Laser (Canadian Pioneer Medical Technology Corporation)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2024: 12025: 1
2024high 1 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Cpmt Laser (Canadian Pioneer Medical Technology Corporation) by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cpmt Laser (Canadian Pioneer Medical…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • GEXPowered Laser Surgical Instrument1decision
  • NGXStimulator, Muscle, Powered, For Muscle Conditioning1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K241601EMS (FlexPulse, MagnaCore, Magnetika)Cpmt Laser (Canadian Pioneer Medical Technology Corporation) · 2025
  • K232133Co2 Laser System, Models: PureLase And VanLaseCpmt Laser (Canadian Pioneer Medical Technology Corporation) · 2024

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