Data / Medical devices / United States / Ilion Medical Inc
Ilion Medical Inc: FDA-registered device maker in Minneapolis, MN, United States, 1 510(k) clearance
Ilion Medical Inc is registered with the FDA (registration 3014919610) in Minneapolis, MN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 5, 2020. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3014919610
- Address
- Medical Arts Building 825 Nicollet Mall, Suite 700, Minneapolis, MN, United States, 55402
- Owner or operator
- Ilion Medical Inc (10088627)
- Roles
- Manufacturer
- First device listed
- September 7, 2023
- Registered through
- 2026
- Brand names listed
- NADIA Sacroiliac Fusion Implant
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Sacroiliac Joint Fixation | OUR | 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 |
|---|---|---|---|---|---|---|
| August 5, 2020 | K190580 | NADIA SI Fusion System | OUR | Substantially Equivalent | Ilion Medical, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 5, 2020. 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.