Data / Medical devices / Chair, Examination And Treatment / Canada
FDA-registered makers of Chair, Examination And Treatment in Canada: 5 establishments
5 establishments in Canada are registered with the FDA to make Chair, Examination And Treatment (product code FRK). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Chair, Examination And Treatment
- Product code
- FRK
- Country
- Canada
Makers of Chair, Examination And Treatment in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Global Upholstery Co. Inc. | Toronto Ontario, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Safari Dental, Inc. | BOISBRIAND Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stance Healthcare Inc | Kitchener Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surface Medical, Inc. | Calgary Alberta, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Upper Cervical Store, Inc. | Calgary Alberta, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.