Data / Medical devices / Canada / Keter Canada Inc.
Keter Canada Inc.: FDA-registered device maker in Milton Ontario, Canada, 2 510(k) clearances
Keter Canada Inc. is registered with the FDA (registration 3010508078) in Milton Ontario, Canada. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated October 14, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010508078
- Address
- 205 Market Drive, Milton Ontario, Canada, L9T 4Z7
- Owner or operator
- Keter Canada, Inc. (10045078)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- June 4, 2014
- Registered through
- 2026
- Brand names listed
- AP 30 DUO (8 Gal DUO lid), AP 30 MONO (8 Gal MONO lid), AP 5.4 QT, AP 50 DUO (12 Gal DUO lid), AP 50 MONO (12 Gal MONO lid), AP 60 DUO (18 Gal DUO lid), AP 60 MONO (18 Gal MONO lid), AP Medical and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Sharps | MMK | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 14, 2025 | K252637 | Community Containers (Flap and Daisy) | MMK | Substantially Equivalent | Keter Canada, Inc. | accessdata.fda.gov |
| April 2, 2008 | K071517 | AP MEDICAL SHARPS CONTAINERS 0,6-12 LT. | MMK | Substantially Equivalent | A.B.M. Italia S.P.A | accessdata.fda.gov |
Compare with other makers
Updated October 14, 2025. 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.