Rambler Mobility, Inc.
Country not established
- Devices
- 1
What Rambler Mobility, Inc. makes
Rambler Mobility, Inc. manufactures the RAMBLER, a mobility assistance device designed for individuals with limited lower-body function. This product is intended to provide active standing and weight-bearing support, aiding in mobility and physical therapy for users.
The RAMBLER is classified as a Class II medical device under FDA regulations and has undergone 510(k) clearance. The company is based in the United States, and its devices are listed in the FDA’s 510(k) registry.
Catalogue
Rambler Ref K011401
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rambler Mobility, Inc. have in the registry?
The registry currently lists 1 device for Rambler Mobility, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rambler Mobility, Inc.'s devices?
Among its 1 most recently registered device, Rambler Mobility, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rambler Mobility, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rambler Mobility, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rambler Mobility, Inc. in the registry?
The most recently registered devices listed for Rambler Mobility, Inc. include RAMBLER.