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On December 9, 2025, Longest Medical’s LGT-2320 Series Low-Frequency Neuromuscular Electrical Stimulators marked a pivotal milestone in global electrotherapy innovation by securing FDA 510(k) clearance under the identification number K252154. This rigorous regulatory approval underscores the series’ adherence to the U.S. Food and Drug Administration’s stringent safety, performance, and clinical effectiveness standards, positioning the devices as trusted solutions for U.S. healthcare providers and patients alike.
Longest Medical announces FDA 510(k) clearance for its LGT-2210DS compression therapy device, validating its safety and effectiveness for U.S. medical use and enabling broader adoption in American healthcare.
A cutting-edge IPC device, it enhances circulation and lymphatic drainage via precise compressions. With a supporting limb and full-body cuffs, it offers versatility with 29 preset modes, user-friendly controls, and a robust design. This milestone reflects Longest Medical’s commitment to innovative solutions, empowering U.S. providers to elevate patient care in rehabilitation and beyond.
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