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# Renovid Surgical 3D-printed Interbody Fusion System Cleared
- URL: https://www.fdaweb.com/renovid-surgical-3d-printed-interbody-fusion-system-cleared/
- Published: 2018-09-26T12:00:00.000Z
- Updated: 2026-09-15T00:34:20.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5142454

FDA has cleared a Renovis Surgical Technologies 510(k) to market the Tesera X Lateral Interbody Fusion System. The device is made using the company’s proprietary 3D-printed titanium alloy, and features a low modulus, load-sharing design with a randomized pore structure to mimic cancellous bone, the company says. It features a 550-micron average pore size and 68% porosity combined with micro-surface roughness within the structure to augmnt bone ongrowth and ingrowth, it says.