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Data / Medical devices / Stimulator, Nerve, Transcutaneous, For Pain Relief / Canada

FDA-registered makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in Canada: 6 establishments

6 establishments in Canada are registered with the FDA to make Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Stimulator, Nerve, Transcutaneous, For Pain Relief
Product code
GZJ
Country
Canada

Makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in Canada

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Center For Pain And Stress Research, Ltd.TORONTO Ontario, CanadaManufacturer1June 17, 2003000api.fda.gov
Electro Therapeutic Devices IncMarkham Ontario, CanadaManufacturer1March 5, 1985000api.fda.gov
Leading Edge MFG. Inc.Langley British Columbia, CanadaManufacturer1August 18, 2009000api.fda.gov
J. Sterling Industries Ltd.Woodbridge Ontario, CanadaContract manufacturer0000api.fda.gov
Thought Technology Ltd.MONTREAL Quebec, CanadaManufacturer0000api.fda.gov
Tone-A-Matic International, Inc.MISSISSAUGA Ontario, CanadaManufacturer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.