Data / Medical devices / Instrument, Manual, Surgical, General Use / Canada
FDA-registered makers of Instrument, Manual, Surgical, General Use in Canada: 6 establishments
6 establishments in Canada are registered with the FDA to make Instrument, Manual, Surgical, General Use (product code MDM). 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
- Instrument, Manual, Surgical, General Use
- Product code
- MDM
- Country
- Canada
Makers of Instrument, Manual, Surgical, General Use in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Batrik Medical Manufacturing Inc. | Lachine Quebec, Canada | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Halifax Biomedical Inc. | Mabou Nova Scotia, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ludlow Technical Products Canada, Ltd. (A Division of Cardinal Health LLC) | GANANOQUE Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Primed Medical Products Inc. | Edmonton Alberta, Canada | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rmac Surgical Inc | Etobicoke Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Southmedic, Inc. | BARRIE Ontario, Canada | Manufacturer | 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.