The US Food and Drug Administration (FDA) has granted 510(k) clearances to Hollywog's new WiTouch and WiTouch Pro wireless remote controlled devices.
The WiTouch devices, which incorporates TENS technology, are designed for the treatment of back pain.
Hollywog president Chuck Thomas said with the approval, WiTouch is available to patients and healthcare professionals who need creative features, high quality and functionality.
"It is exciting to finalize our FDA clearance and prepare for immediate launch into the US market, as well as our international distribution networks throughout the world," Thomas added.
"I am proud that Hollywog is able to produce both devices here in Chattanooga, TN."
The company said WiTouch and WiTouch Pro devices are available in the US through Core Products, a manufacturer and provider of therapeutic products.
