Amy West
Country not established
- Devices
- 1
What Amy West makes
Amy West manufactures neuromuscular stimulators that integrate ultrasound and muscle activation technologies. These devices are designed for therapeutic applications targeting muscle stimulation, rehabilitation, and pain management. The portfolio includes systems that combine electrical stimulation with ultrasound imaging to assess and treat soft tissue conditions. Products are tailored for clinical and home-use settings to enhance recovery and mobility.
The company’s neuromuscular stimulators fall under Class II regulatory classification in the US, requiring 510(k) clearance through the FDA. These devices are listed in the FDA’s 510(k) Premarket Notification Database as authorised medical instruments. Amy West operates from the United States, adhering to domestic regulatory standards for neuromuscular stimulation technologies.
Catalogue
Stimulator, Ultrasound And Muscle Ref K871647
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amy West have in the registry?
The registry currently lists 1 device for Amy West. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amy West's devices?
Among its 1 most recently registered device, Amy West has devices listed in FDA 510(k) (1 device).
What risk classes do Amy West's devices fall under?
Among its 1 most recently registered device, the classes recorded for Amy West's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amy West in the registry?
The most recently registered devices listed for Amy West include STIMULATOR, ULTRASOUND AND MUSCLE.