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Data / Medical devices / Orthopedic Stereotaxic Instrument / Canada

FDA-registered makers of Orthopedic Stereotaxic Instrument in Canada: 7 establishments

7 establishments in Canada are registered with the FDA to make Orthopedic Stereotaxic Instrument (product code OLO). 3 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device
Orthopedic Stereotaxic Instrument
Product code
OLO
Country
Canada

Makers of Orthopedic Stereotaxic Instrument in Canada

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Zimmer CasMontreal, Quebec, CanadaManufacturer, Specification developer17May 21, 2026040api.fda.gov
7D Surgical ULCToronto Ontario, CanadaManufacturer, Specification developer7May 20, 2022000api.fda.gov
Intellijoint Surgical Inc.Kitchener Ontario, CanadaManufacturer2October 1, 2019030api.fda.gov
A7 IntegrationGranby Quebec, CanadaContract manufacturer0000api.fda.gov
Engineering CPR Inc.mississauga Ontario, CanadaContract manufacturer0000api.fda.gov
Northern Digital, Inc.WATERLOO Ontario, CanadaComplaint file establishment, Exporter to the US, Specification developer0000api.fda.gov
Nse-AutomatechGranby Quebec, CanadaContract 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.