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Data / Medical devices / Transducer, Ultrasonic, Diagnostic / Canada

FDA-registered makers of Transducer, Ultrasonic, Diagnostic in Canada: 8 establishments

8 establishments in Canada are registered with the FDA to make Transducer, Ultrasonic, Diagnostic (product code ITX). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Transducer, Ultrasonic, Diagnostic
Product code
ITX
Country
Canada

Makers of Transducer, Ultrasonic, Diagnostic in Canada

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Exact Imaging, Inc.Markham Ontario, CanadaExporter to the US, Manufacturer, Specification developer1April 21, 1999000api.fda.gov
National Therapy Products Inc.Brampton Ontario, CanadaManufacturer1October 18, 2001000api.fda.gov
Clarius Mobile Health Corp.Vancouver British Columbia, CanadaComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
Conavi Medical IncToronto Ontario, CanadaManufacturer0000api.fda.gov
Fujifilm Visualsonics, Inc.TORONTO Ontario, CanadaSpecification developer0000api.fda.gov
Sonele Inc.Markham Ontario, CanadaContract manufacturer0000api.fda.gov
Sonic Incytes Medical CorpVancouver British Columbia, CanadaComplaint file establishment, Manufacturer0000api.fda.gov
Ventripoint Diagnostics Ltd.Toronto Ontario, CanadaComplaint file establishment, Manufacturer0000api.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.