Data / Medical devices / United States / Si Solutions
Si Solutions: FDA-registered device maker in Columbia, MO, United States, 1 510(k) clearance
Si Solutions is registered with the FDA (registration 3042024509) in Columbia, MO, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 20, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042024509
- Address
- 1010 Club Village Dr Ste C, Columbia, MO, United States, 65203
- Owner or operator
- SI Solutions (10094337)
- Roles
- Specification developer
- First device listed
- November 24, 2025
- Registered through
- 2026
- Brand names listed
- OPTUMSI SACROILIAC JOINT IMPLANT
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Sacroiliac Joint Fixation | OUR | 2 | 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 |
|---|---|---|---|---|---|---|
| November 20, 2025 | K251365 | OptumSI Implant System | OUR | Substantially Equivalent | Si Solutions, LLC | accessdata.fda.gov |
Compare with other makers
Updated November 20, 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.