Freeman Procedure Seminars
Country not established
- Devices
- 1
What Freeman Procedure Seminars makes
Freeman Procedure Seminars manufactures the ArthroStim Manipulator, a device designed for joint manipulation and mobilization, commonly used in orthopedic and physical therapy settings to assist with arthrokinematic techniques.
The ArthroStim Manipulator is classified as Class II (U) under FDA regulations and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Arthrostim Manipulator Ref K930431
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Freeman Procedure Seminars have in the registry?
The registry currently lists 1 device for Freeman Procedure Seminars. Devices recorded under merged duplicate company entries are counted once.
Which registries list Freeman Procedure Seminars's devices?
Among its 1 most recently registered device, Freeman Procedure Seminars has devices listed in FDA 510(k) (1 device).
What are the newest devices from Freeman Procedure Seminars in the registry?
The most recently registered devices listed for Freeman Procedure Seminars include ARTHROSTIM MANIPULATOR.