Patients
Providers
- Prescription Form
How to Use
Our Products
Visit Our Clinic
Contact Us

Licenses & Certifications

The InterX 1000 is FDA cleared for:

symptomatic relief and management of chronic intractable pain
adjunctive treatment in the management of post-surgical and post-traumatic pain.

InterX Technologies is an ISO 13485 Registered company.

*The InterX® Neurostimulation System is patented technology for the devices and the accessory electrodes. It is FDA cleared for symptomatic relief and management of chronic intractable pain, and adjunctive treatment in the management of post-surgical and post-traumatic pain. The FDA has not approved or cleared InterX® devices as safe or effective for any other uses. Is ISO13485 Registered company. CSA certified.

Supplier Quality Requirements

One Year Warranty Policy