Data / Medical devices / United States / Aoa Products LLC
Aoa Products LLC: FDA-registered device maker in Toledo, OH, United States, 1 510(k) clearance
Aoa Products LLC is registered with the FDA (registration 3007630531) in Toledo, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 14, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007630531
- Address
- 3618 King RD. Unit D, Toledo, OH, United States, 43617
- Owner or operator
- AOA PRODUCTS LLC (10095135)
- Roles
- Repackager or relabeler
- First device listed
- January 27, 2026
- Registered through
- 2026
- Brand names listed
- syngo Dymamics
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Automated Radiological Image Processing Software | QIH | 2 | Repackager or relabeler | 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 14, 2022 | K222428 | Syngo Dynamics (Version VA40F) | QIH | Substantially Equivalent | Siemens Medical Solutions USA, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 14, 2022. 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.