Clearance expands Company's competitive advantage of clinically proven, minimally invasive technologies to treat debilitating ...

Tenon Medical’s SImmetry+ sacroiliac joint fusion system earned the FDA’s 510(k) clearance, according to an Oct. 21 news release. The SImmetry+ system is a minimally invasive lateral access system ...

Sacroiliac joint fusions had no complications when performed by spine surgeons and low complication rates when performed by pain physicians, according to a study published in the November 2025 issue ...

1. Tenon Medical earned FDA 510(k) clearance to use its Catamaran sacroiliac joint system for augmenting thoracolumbar fusion. The indication was first used in June by Andrew Trontis, MD. 2. A new ...

DEL MAR, Calif.--(BUSINESS WIRE)--SAIL Fusion, a medical device company focused on advancing the surgical treatment of sacroiliac joint dysfunction through solutions built upon AO principles, today ...

DEL MAR, Calif.--(BUSINESS WIRE)--SAIL Fusion, a medical device company focused on advancing the surgical treatment of sacroiliac joint dysfunction through solutions built upon proven AO principles, ...

Tenon Medical (TNON) has received U.S. Food and Drug Administration 510(k) clearance for the SImmetry+ SI Joint Fusion System. The SImmetry+ ...

Clearance expands Company's competitive advantage of clinically proven, minimally invasive technologies to treat debilitating SI joint conditions from multiple surgical approaches~~SImmetry+'s New 3D ...