The next-gen TLIF implant is engineered to maximize performance in both traditional open procedures, as well as with endoscopic approaches.

ReConnex is a ready-to-use, FDA 510(k)-cleared device designed to help simplify all-inside anterior cruciate ligament reconstruction.

Miach Orthopaedics initiated the Bridge Registry to assess real-world outcomes for the Bridge-Enhanced ACL Restoration (BEAR) Implant.

Sourced from bovine achilles tendon, the Type 1 collagen used in the wound dressing leverages robust biological properties that support tissue regeneration and repair.

Newton converts soft tissue dynamics into actionable intraoperative guidance, supporting more consistent and reproducible surgical execution.

The U.S. Phase III trial expands the investigation of umbilical cord therapy for symptomatic cartilage defects due to knee OA.

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.