Meet Cala kIQ — the only FDA-cleared, wearable device that delivers effective therapy for action hand tremor in people with essential tremor and Parkinson’s disease. Is it for me? Answer a few questions and find out if the Cala kIQ System could work for you.

Understanding the Context

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Key Insights

Food and Drug Administration (FDA) has cleared the Cala kIQ Plus system, the next-generation of its wearable neurostimulation device for action hand tremor in essential tremor (ET) and Parkinson's disease (PD). The Cala kIQ Plus introduces new therapy modes and adaptive calibration designed to optimize tremor relief and ... The Cala kIQ Plus provides new therapy modes and adaptive calibration designed to optimize tremor relief and personalize treatment Data to be presented at American Academy of Neurology Meeting in Chicago, April 18-22 SAN MATEO, Calif. and CHICAGO, /PRNewswire/ -- Cala ®, the bioelectronic medicine leader, today announced U.S. Food and Drug Administration (FDA) clearance of the ...

Final Thoughts

Cala announced today that it received FDA clearance for its kIQ Plus next-generation wearable neurostimulation device. Cala Motors LLC is a business entity based in Kissimmee, FL. Established recently on , this Florida Limited Liability Company is recognized under the document number L24000400455. Effectively manage your cala device therapy. Find the freedom to focus on life. CALA and ANAB have signed a strategic partnership to offer laboratories collaborative accreditation.

This collaboration supports laboratories in gaining broader market access, regulatory recognition, and increased trust from clients across North America.