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MY01 has developed and commercialized a continuous compartmental pressure monitoring device for the early and accurate diagnosis of acute compartment syndrome. The company’s device is FDA-cleared, CE-marked, and has received Breakthrough Device Designation. Clinical studies have demonstrated its safety and functionality in trauma patients at risk for developing compartment syndrome. As of March 2025, the company had shipped over 2,000 devices with use in more than 2,000 patients[1][4][5].
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