Data / Medical devices / Applicator, Absorbent Tipped, Non-Sterile / Canada
FDA-registered makers of Applicator, Absorbent Tipped, Non-Sterile in Canada: 5 establishments
5 establishments in Canada are registered with the FDA to make Applicator, Absorbent Tipped, Non-Sterile (product code KXF). 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
- Applicator, Absorbent Tipped, Non-Sterile
- Product code
- KXF
- Country
- Canada
Makers of Applicator, Absorbent Tipped, Non-Sterile in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| AMD Medicom Inc. | Pointe-Claire, Montreal Quebec, Canada | Complaint file establishment, Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beyes Dental Inc | Toronto Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bio Nuclear Diagnostics, Inc. | TORONTO Ontario, Canada | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dna Genotek, Inc. | Ottawa Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Iris Beauty Supplies Inc | DOLLARD-DES-ORMEAUX Quebec, 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.