Compex Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Staodyn Max Preset, Model 4470 Ref K061516
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Compex Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Compex Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Compex Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Compex Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Compex Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Compex Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Compex Technologies, Inc. in the registry?
The most recently registered devices listed for Compex Technologies, Inc. include REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S and STAODYN MAX PRESET, MODEL 4470.