Data / Medical devices / United States / Advahealth Solutions
Advahealth Solutions: FDA-registered device maker in Minneapolis, MN, United States, 1 510(k) clearance
Advahealth Solutions is registered with the FDA (registration 3044519982) in Minneapolis, MN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 17, 2024. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3044519982
- Address
- 331 2nd Ave S Ste 400, Minneapolis, MN, United States, 55401
- Owner or operator
- AdvaHealth Solutions (10093427)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- May 22, 2025
- Registered through
- 2027
- Brand names listed
- AdvaView
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| January 17, 2024 | K233226 | FlexView Diagnostic (v1.1.20) | LLZ | Substantially Equivalent | Radical Imaging, LLC | accessdata.fda.gov |
Compare with other makers
Updated January 17, 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.