The platform is designed to address the operational barriers that may limit minimally invasive spine surgery.

The implant is a knitted surgical scaffold in the form of a band intended to provide fixation during the healing process following syndesmotic trauma.

The naturally-derived hyaluronic acid and alginate hydrogel is designed to provide a conformable, bioresorbable gliding interface.

Lantern ASC includes a reusable navigation unit paired with a procedural Smart Pack Kit to integrate into existing surgical workflows.

NanoCept coating technology is intended to mitigate bacterial contamination on the implant surface prior to implantation.

The Saber-C system combines the stability of traditional anterior cervical plating with a zero-profile interbody construct.

VersaLift offers one of the smallest starting heights available for a TLIF expandable interbody implant, beginning at just 6mm.

MISHA is shown to be effective for knee OA patients who failed non-surgical treatments, but are not indicated or are unwilling to get a knee replacement.

The project is on track to reach the next milestone toward CE Mark approval of HyProtect-coated revision implants.

FDA approved an IDE application for a pivotal clinical trial of SOLA-2 Alternating Magnetic Field System in patients with periprosthetic joint infections.