Data / Medical devices / Container, Specimen Mailer And Storage, Non-Sterile / Canada
FDA-registered makers of Container, Specimen Mailer And Storage, Non-Sterile in Canada: 9 establishments
9 establishments in Canada are registered with the FDA to make Container, Specimen Mailer And Storage, Non-Sterile (product code NNK). 0 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
- Container, Specimen Mailer And Storage, Non-Sterile
- Product code
- NNK
- Country
- Canada
Makers of Container, Specimen Mailer And Storage, Non-Sterile in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Dna Genotek, Inc. | Ottawa Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Genetrack Biolabs Inc. | Vancouver British Columbia, Canada | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Imperial Surgical Ltd. | Lachine Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| L-D Tool & Die Division Of Madix Engineering | Ottawa Ontario, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Les Plastiques MDJ Inc. | Saint-Hubert Quebec, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Liquimedlock | Markham Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pretium Canada Packaging ULC | ETOBICOKE Ontario, Canada | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Primed Instruments, Inc. | MISSISSAUGA Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Simport Scientific Inc. | BELOEIL Quebec, Canada | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.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.