Wandercraft
FranceFDA applicant, unverified FDA FEI 3015000676
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Eve Ref K260381
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015000676
- DUNS number
- 264523488
- Address
- 23-23 bis avenue d'Italie, Paris Ile-de-France
- Website
- www.wandercraft.eu
- linkedin.com/company/wandercraft
- facebook.com/wandercraft.eu
- [email protected]
From the company website
Wandercraft builds self-balancing robotic exoskeletons and humanoid robots so people can do what they can't.
Frequently asked questions
How many devices does Wandercraft have in the registry?
The registry currently lists 1 device for Wandercraft. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wandercraft's devices?
Among its 1 most recently registered device, Wandercraft has devices listed in FDA 510(k) (1 device).
What risk classes do Wandercraft's devices fall under?
Among its 1 most recently registered device, the classes recorded for Wandercraft's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wandercraft in the registry?
The most recently registered devices listed for Wandercraft include Eve.