Global Muscle Stimulation Devices Market: Key Developments
In May 2021, ITO CO., LTD., is Japan-based engineering and manufacturers and electrophysical agents announced that electrical muscle stimulator for TMJ (temporomandibular joint) Pain Relief "D function" had received 510(k) clearance by the U.S. FDA. Its use for Prevents and reveres muscle atrophy (loss of muscle mass/tissue) Enhances rehabilitation of muscles. Increases range of motion for tense muscles or tendons. Reduces stress and discomfort.
In September 2021, NCS America, Inc., is a medical technology company announced that U.S. Food and Drug Administration (FDA) cleared the Shoulder Pacemaker and its unique Motion Activated Stimulation (MAS) technology. The Shoulder Pacemaker is an innovative wearable electro stimulator created for patients suffering from unbalanced muscle activation in the shoulder.
In October 2022, Medtronic is a medical technology, services, and solutions. The Company launched Medtronic Neurovascular Co-Lab Platform to accelerate innovation in stroke treatment. Neurovascular Co-Lab Platform drives collaboration and connections among start-ups, physicians, and institutions; aims to improve stroke treatment and access for patients worldwide.
In July 2021, Neurolief, an Israel-based neuromodulation company and NeuroFront, a clinical stage biotech company, announced an exclusive licensing agreement for NeuroFront to develop and commercialize Relivion, non-invasive medical devices for the treatment of migraine and depression, in China and South Korea.
Joining thousands of companies around the world committed to making the Excellent Business Solutions.
View All Our Clients