Data / Medical devices / Neurological Stereotaxic Instrument / Canada
FDA-registered makers of Neurological Stereotaxic Instrument in Canada: 9 establishments
9 establishments in Canada are registered with the FDA to make Neurological Stereotaxic Instrument (product code HAW). 5 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Neurological Stereotaxic Instrument
- Product code
- HAW
- Country
- Canada
Makers of Neurological Stereotaxic Instrument in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Zimmer Cas | Montreal, Quebec, Canada | Manufacturer | 9 | July 20, 2007 | 0 | 4 | 0 | api.fda.gov |
| Synaptive Medical Inc | Mississauga Ontario, Canada | Exporter to the US, Manufacturer | 5 | July 14, 2019 | 0 | 2 | 1 | api.fda.gov |
| 7D Surgical ULC | Toronto Ontario, Canada | Manufacturer, Specification developer | 4 | December 27, 2024 | 0 | 0 | 0 | api.fda.gov |
| ClaroNav Inc. | Toronto Ontario, Canada | Manufacturer | 2 | February 5, 2025 | 0 | 0 | 0 | api.fda.gov |
| Northern Digital, Inc. | WATERLOO Ontario, Canada | Complaint file establishment, Exporter to the US, Specification developer | 2 | July 14, 2010 | 0 | 2 | 0 | api.fda.gov |
| Engineering CPR Inc. | mississauga Ontario, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Exo-s Saint-Damien Inc. | St-Damien de Buckland Quebec, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nse-Automatech | Granby Quebec, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Starfish Product Engineering | Toronto Ontario, Canada | Contract 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.