Data / Medical devices / Cleaner, Ultrasonic, Medical Instrument / Canada
FDA-registered makers of Cleaner, Ultrasonic, Medical Instrument in Canada: 6 establishments
6 establishments in Canada are registered with the FDA to make Cleaner, Ultrasonic, Medical Instrument (product code FLG). 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
- Cleaner, Ultrasonic, Medical Instrument
- Product code
- FLG
- Country
- Canada
Makers of Cleaner, Ultrasonic, Medical Instrument in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Armstrong Manufacturing Incorporated | Mississauga Ontario, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Germiphene Corp. | BRANTFORD Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maxill, Inc. | ST. THOMAS Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Micrylium Laboratories Inc. | TORONTO Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scican Ltd. | TORONTO Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Southmedic, Inc. | BARRIE Ontario, Canada | Complaint file establishment, Foreign private label distributor, 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.