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Canadian Pioneer Medical Technology Corporation

FDA Regulatory Profile

Canadian Pioneer Medical Technology Corporation has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Feb 25, 2022

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances3Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K211722Laser treatment system , models Nyx plus, Grace plus, Nemesis, AresFeb 25, 2022
K212793Laser Treatment System, Model: Hera, ArmoOct 25, 2021
K210033Laser Treatment System, Model: NYX and GraceFeb 26, 2021

FDA data resources