Data / Medical devices / Canada / Velox Manufacturing Inc.
Velox Manufacturing Inc.: FDA-registered device maker in Langley British Columbia, Canada, 1 510(k) clearance
Velox Manufacturing Inc. is registered with the FDA (registration 3030927010) in Langley British Columbia, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 12, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030927010
- Address
- 23790 36A Ave, Langley British Columbia, Canada, V2Z2J6
- Owner or operator
- Velox Manufacturing Inc. (10090579)
- Roles
- Manufacturer
- First device listed
- April 15, 2024
- Registered through
- 2026
- Brand names listed
- Velox MPC
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Powered | ITI | 2 | 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 |
|---|---|---|---|---|---|---|
| January 12, 2024 | K231315 | Velox Power Chair | ITI | Substantially Equivalent | Velox Manufacturing, Inc. | accessdata.fda.gov |
Compare with other makers
Updated January 12, 2024. 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.