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Data / Medical devices / Shield, Protective, Personnel / Canada

FDA-registered makers of Shield, Protective, Personnel in Canada: 8 establishments

8 establishments in Canada are registered with the FDA to make Shield, Protective, Personnel (product code KPY). 0 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
Shield, Protective, Personnel
Product code
KPY
Country
Canada

Makers of Shield, Protective, Personnel in Canada

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Armery Medical Technologies Inc.London Ontario, CanadaContract manufacturer, Specification developer0000api.fda.gov
BWXT Medical Ltd.OTTAWA Ontario, CanadaContract manufacturer0000api.fda.gov
Instrumed SurgicalMississauga Ontario, CanadaManufacturer0000api.fda.gov
Lemer Pax AmericaMontreal Quebec, CanadaContract manufacturer, Manufacturer0000api.fda.gov
Primed Medical Products Inc.Edmonton Alberta, CanadaSpecification developer0000api.fda.gov
South West Exposures (2566031 Ont Inc.)Toronto Ontario, CanadaContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Tornado PlasticsSt-Laurent Quebec, CanadaManufacturer0000api.fda.gov
Ultraray Group Inc.Oakville 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.