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# FDA Clears Misonix 510(k) for Nexus
- URL: https://www.fdaweb.com/fda-clears-misonix-510-k-for-nexus/
- Published: 2019-06-04T12:00:00.000Z
- Updated: 2026-09-15T01:30:32.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5144255

FDA has cleared a Misonix 510(k) for Nexus, an ultrasonic surgical platform. The company says its next-generation integrated device combines all the features of Misonix’s existing features, including BoneScalpel, SonicOne and Sonastar, into an integrated platform that will also serve to power future options. Nexus is driven by a new proprietary digital algorithm that results in more power, efficiency and control, Misonix says, adding that it incorporates radiofrequency capabilities for general surgery procedures. The device also features increased power to improve tissue resection rates and bone removal.