Dane Technologies
United Statesfrom the FDA registration address FDA FEI 3003857817
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Dane Technologies makes
Dane Technologies manufactures the Wheelchair Mover (Model WM 2000), a device designed to assist in the transfer and repositioning of wheelchair users.
The Wheelchair Mover is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003857817
- Address
- 10400 Fountains Drive, Maple Grove, MN, 55369
Frequently asked questions
How many devices does Dane Technologies have in the registry?
The registry currently lists 1 device for Dane Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dane Technologies's devices?
Among its 1 most recently registered device, Dane Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Dane Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dane Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dane Technologies in the registry?
The most recently registered devices listed for Dane Technologies include DANE TECHNOLOGIES WHEELCHAIR MOVER, MODEL WM 2000.