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Data / Medical devices / Container, Specimen, Sterile / Canada

FDA-registered makers of Container, Specimen, Sterile in Canada: 8 establishments

8 establishments in Canada are registered with the FDA to make Container, Specimen, Sterile (product code FMH). 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
Container, Specimen, Sterile
Product code
FMH
Country
Canada

Makers of Container, Specimen, Sterile in Canada

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bio Nuclear Diagnostics, Inc.TORONTO Ontario, CanadaExporter to the US, Manufacturer0000api.fda.gov
Les Plastiques MDJ Inc.Saint-Hubert Quebec, CanadaContract manufacturer, Repackager or relabeler0000api.fda.gov
LiquimedlockMarkham Ontario, CanadaManufacturer0000api.fda.gov
Pretium Canada Packaging ULCETOBICOKE Ontario, CanadaContract manufacturer, Manufacturer0000api.fda.gov
Simport Scientific Inc.BELOEIL Quebec, CanadaForeign private label distributor, Manufacturer, Specification developer0000api.fda.gov
Southmedic, Inc.BARRIE Ontario, CanadaContract manufacturer0000api.fda.gov
Verathon Medical (canada) ULCBurnaby British Columbia, CanadaSpecification developer0000api.fda.gov
Verathon Medical (canada) ULC.BURNABY British Columbia, 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.