Exactech, a global medical technology leader, announced today it has received 510(k) clearance from the U.S. Food and Drug ...

Exactech announced today that it received FDA 510(k) clearance for its Truliant porous tibial tray, a 3D tibial knee implant.

The U.S. Food and Drug Administration (FDA) has granted 510 (k) clearance to a standalone lateral lumbar interbody fusion ...

The results from a retrospective study of 50 patients with systemic lupus erythematosus (SLE) and osteonecrosis of the femoral head suggest that free vascularized fibular grafting offers a viable ...

The implant utilises additive manufacturing techniques to create a porous structure that resembles a cancellous bone ...

A potential advantage of the jail technique is the prevention of screw cut-outs through the cancellous bone.

Neoss Inc., a leading innovator in dental implant solutions and digital workflows, is excited to extend its line of ...

Discover Exactech's latest innovation in knee replacement surgery with the FDA clearance of Truliant Porous Tibial Tray, featuring advanced 3D technology.