Kinesthetics, Inc.
Country not established
- Devices
- 1
What Kinesthetics, Inc. makes
Kinesthetics, Inc. manufactures the KINESTHETICS Model 2000 NMS, a device designed for neuromuscular stimulation and rehabilitation applications, targeting muscle activation and recovery.
The company’s portfolio is regulated under FDA Class II devices, with the Model 2000 NMS authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Kinesthetics Model 2000 Nms Ref K903870
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinesthetics, Inc. have in the registry?
The registry currently lists 1 device for Kinesthetics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinesthetics, Inc.'s devices?
Among its 1 most recently registered device, Kinesthetics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kinesthetics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kinesthetics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinesthetics, Inc. in the registry?
The most recently registered devices listed for Kinesthetics, Inc. include KINESTHETICS MODEL 2000 NMS.