current Interx system
fda 510(k) class ii medical devices
InterX 5002 and InterX 1000 devices are Class II Medical Devices with 510(k) clearance by the US FDA for the indications of symptomatic relief and management of chronic intractable pain and adjunctive treatment in the management of post surgical and post traumatic pain and carries GSA Military Approval and the European CE Mark. US Patent No. 9, 630, 003 B2
The non-invasive neuro stimulation system patents encompass InterX 5002, InterX 1000 and electrode accessories that interface with both of these devices.
non-invasive neuro stimulation
Currently marketed in the USA and internationally
InterX InterX 5002 and InterX 1000 devices are used to apply an electric pulse or spike to a patient to treat the patient. Devices have a series of preset treatments programmed therein. A user can select a treatment from menus displayed on a display. A variety of probes can be used with the devices, with the device automatically detecting the type of probe attached. Multiple electrodes can be used on the probe, which allows the active areas in contact with the probe to be identified prior to treatment to allow the treatment to concentrate on the active areas.
With the InterX 5002 Professional Device impedance of the skin and underlying tissue to be treated can be measured prior to the treatment to locate active areas on the skin for treatment.