Springbok, Inc.
Country not established
- Devices
- 2
What Springbok, Inc. makes
Springbok, Inc. manufactures the MuscleView, a diagnostic imaging device designed for visualizing muscle tissue and assessing musculoskeletal conditions.
The MuscleView is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
MuscleView Ref K241331
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 079158113
Frequently asked questions
How many devices does Springbok, Inc. have in the registry?
The registry currently lists 2 devices for Springbok, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Springbok, Inc.'s devices?
Among its 2 most recently registered devices, Springbok, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Springbok, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Springbok, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Springbok, Inc. in the registry?
The most recently registered devices listed for Springbok, Inc. include MuscleView 2.0 and MuscleView.