Altior Trauma Announces FDA 510(K) Clearance for the Artemis Proximal Femoral Nail System

NEW LONG NAIL TO STRENGTHEN THE ARTEMIS SYSTEM AND STREAMLINE WORKFLOWS ENGLEWOOD CLIFFS, NJ, USA, October 31, 2022 / – Altior Trauma a GLW, Inc. company, (“Altior Trauma”), a medical device company focused on a paradigm shift in the surgical treatment of trochanteric hip fractures, announced today an additional U.S. Food and Drug Administration (FDA) 510(k) clearance … Continued

Carbon22 Receives FDA 510(k) Clearance for Apollo™ Ankle Fracture Plating System

Englewood Cliffs, NJ., — Carbon22™, a GLW, Inc. medical technology company with a focus on the foot and ankle orthopedic market, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its upcoming Apollo Ankle Fracture Plating System, a novel portfolio of see-through, “ortholucent” bone plates and screws used … Continued

Solvay and Carbon22™ partner on Creed™ Cannulated Screws for orthopedics

Alpharetta, Ga., — Solvay’s Zeniva® polyetheretherketone (PEEK) resin was chosen by Carbon22™, a GLW, Inc. company, for its new Creed™ Cannulated Screw System for foot and ankle surgery. This advanced new screw system recently received 510(k) clearance from the U.S. Food and Drug Administration (FDA).  To create the new system’s ortholucent, plastic-metal hybrid composite, Solvay’s implant-grade radiolucent Zeniva® PEEK resin … Continued