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# FDA Clears I-Bone’s iFuse 3D Implant
- URL: https://www.fdaweb.com/fda-clears-i-bones-ifuse-3d-implant/
- Published: 2017-06-13T12:00:00.000Z
- Updated: 2026-09-14T22:28:54.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5138925

FDA has cleared an I-Bone 510(k) for the iFuse-3D Implant, which the company describes as the first 3D-printed titanium implant for use in the sacroiliac joint. The company says it developed a proprietary 3D-printing technology “to create an implant with a unique patented fenestrated design and enhanced porous surface that resembles the trabecular structure of cancellous bone. Together, these two features provide an excellent environment for bony ongrowth, ingrowth and through growth.” The device’s surface and fenestrated structure were designed to provide enhanced osteointegration and promote intra-articular fusion, it says.