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# FDA Clears MX Ortho dynaMX Staple
- URL: https://www.fdaweb.com/fda-clears-mx-ortho-dynamx-staple/
- Published: 2016-02-10T12:00:00.000Z
- Updated: 2026-09-15T02:34:57.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5134727

> FDA has cleared an MX Orthopedics 510(k) for the dynaMX Compression Staple for fracture fixation. The device, which is made of “superelastic nitinol,” allows the surgeon to control the opening of staple legs, according to the company. There is no post-insertion tamping required, and it allows easy intraoperative removal (if needed), it says.