Wallant Intl. Trade, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Wallant Intl. Trade, Inc. makes
Wallant Intl. Trade, Inc. makes automatic electrode placement belts and TENS devices, including the Wallant Neurologix General Purpose TENS and the Wallant Neurologix Dual Pur Nerve/Neuromuscular Stimulator.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Automatic Electrode Placement Belt Ref K810262
Regimes: 510(k) Registry: 510(k)Wallant Neurologix General Purpose Tens Ref K860847
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wallant Intl. Trade, Inc. have in the registry?
The registry currently lists 3 devices for Wallant Intl. Trade, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wallant Intl. Trade, Inc.'s devices?
Among its 3 most recently registered devices, Wallant Intl. Trade, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Wallant Intl. Trade, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Wallant Intl. Trade, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wallant Intl. Trade, Inc. in the registry?
The most recently registered devices listed for Wallant Intl. Trade, Inc. include AUTOMATIC ELECTRODE PLACEMENT BELT, WALLANT NEUROLOGIX GENERAL PURPOSE TENS and WALLANT NEUROLOGIX DUAL PUR NERVE/NEUROMUSCU STIMU.