Data / Medical devices / Canada / Neuro Spinal Innovation Inc (nsi)
Neuro Spinal Innovation Inc (nsi): FDA-registered device maker in Mississauga Ontario, Canada, 1 510(k) clearance
Neuro Spinal Innovation Inc (nsi) is registered with the FDA (registration 3042251731) in Mississauga Ontario, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 15, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3042251731
- Address
- 77 City Centre Drive Suite 501, East Tower, Mississauga Ontario, Canada, L5B 1M5
- Owner or operator
- Neuro Spinal Innovation Inc (NSI) (10094278)
- Roles
- Specification developer
- First device listed
- November 21, 2025
- Registered through
- 2026
- Brand names listed
- SONIK MONARK 100
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Manipulator, Plunger-Like Joint | LXM | U | Specification developer | 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 |
|---|---|---|---|---|---|---|
| February 15, 2024 | K234036 | SONIK MONARK 100 | LXM | Substantially Equivalent | Neuro Spinal Innovation, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 15, 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.