Data / Medical devices / United States / Dane Technologies
Dane Technologies: FDA-registered device maker in Maple Grove, MN, United States, 1 510(k) clearance
Dane Technologies is registered with the FDA (registration 3003857817) in Maple Grove, MN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 28, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003857817
- Address
- 10400 Fountains Drive, Maple Grove, MN, United States, 55369
- Owner or operator
- DANE TECHNOLOGIES (9077419)
- Roles
- Manufacturer
- First device listed
- September 7, 2010
- Registered through
- 2026
- Brand names listed
- WheelChair Mover
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Powered | ITI | 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 |
|---|---|---|---|---|---|---|
| January 28, 2008 | K073701 | DANE TECHNOLOGIES WHEELCHAIR MOVER, MODEL WM 2000 | ITI | Substantially Equivalent | Dane Technologies | accessdata.fda.gov |
Compare with other makers
Updated January 28, 2008. 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.