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# SurGenTec Sacroiliac Joint Fusion Device Cleared
- URL: https://www.fdaweb.com/surgentec-sacroiliac-joint-fusion-device-cleared/
- Published: 2023-06-09T12:00:00.000Z
- Updated: 2026-09-14T18:38:12.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5154662

FDA has cleared a SurGenTec 510(k) for its TiLink-L Sacroiliac Joint Fusion System, a device that can be implanted from a lateral or posterior/oblique approach. The company says the device’s design allows for superior compression across the joint, and it features SurGenTec’s proprietary Nanotex surface technology to optimize bone growth.

“In-vivo studies conducted by a Good Laboratory Practice facility demonstrated bony in-growth and on-growth which may enhance stability for improved surgical outcomes,” the company says. “The product also boasts a helical self-harvesting channel to capture the patient’s own bone and encourage healing. Graft windows are strategically placed between threads to allow for potential fusion through the screw to enhance stability.”