Data / Medical devices / Canada / Emovi Inc.
Emovi Inc.: FDA-registered device maker in Montreal Quebec, Canada, 1 510(k) clearance
Emovi Inc. is registered with the FDA (registration 3010070342) in Montreal Quebec, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 26, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010070342
- Address
- 4000 rue St-Ambroise, suite 389, Montreal Quebec, Canada, H4C 2C7
- Owner or operator
- Emovi inc. (10044603)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- July 2, 2013
- Registered through
- 2026
- Brand names listed
- KneeKG System, KneeKG attachment system
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Interactive Rehabilitation Exercise Devices | LXJ | 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 26, 2009 | K091000 | KNEEKG | LXJ | Substantially Equivalent | Emovi | accessdata.fda.gov |
Compare with other makers
Updated October 26, 2009. 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.