Two companies recently announced that they have received (510)k clearance from the US Food and Drug Administration (FDA) for 3D printed titanium spinal implants. While Camber Spine Technologies from Pennsylvania received FDA clearance for its SPIRA Open Matrix ALIF device, an interbody fusion implant; the other one was Renovis Surgical Technologies from California for its posterior lumbar Tesera porous titanium interbody fusion systems.