Data / Medical devices / United States / Soul Mobility, Inc
Soul Mobility, Inc: FDA-registered device maker in Oconomowoc, WI, United States, 1 510(k) clearance
Soul Mobility, Inc is registered with the FDA (registration 3035111592) in Oconomowoc, WI, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 12, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3035111592
- Address
- 659 River Bluff Cir, Oconomowoc, WI, United States, 53066
- Owner or operator
- Soul Mobility, Inc (10092545)
- Roles
- Specification developer
- First device listed
- January 18, 2025
- Registered through
- 2026
- Brand names listed
- PFX1214, PFX1517, PFX1820
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Powered | ITI | 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 12, 2024 | K242430 | Power-Flex (PFX1214); Power-Flex (PFX1517); Power-Flex (PFX1820) | ITI | Substantially Equivalent | Soul Mobility | accessdata.fda.gov |
Compare with other makers
Updated November 12, 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.