Activator Methods, Inc.
Country not established
- Devices
- 1
What Activator Methods, Inc. makes
Activator Methods, Inc. manufactures the ACTIVATOR II, a manual orthopedic manipulation device designed for spinal adjustments and musculoskeletal therapy.
The ACTIVATOR II is classified as a Class II (U) device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Activator Ii Ref K973506
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Activator Methods, Inc. have in the registry?
The registry currently lists 1 device for Activator Methods, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Activator Methods, Inc.'s devices?
Among its 1 most recently registered device, Activator Methods, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Activator Methods, Inc. in the registry?
The most recently registered devices listed for Activator Methods, Inc. include ACTIVATOR II.