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GLW Medical Advances Its Ortholucent MIS Platform with GLW Valerius™ Lapidus Bunion System

By orthoPro

GLW Valerius extends GLW Medical’s percutaneous-first bunion portfolio, bringing a Case Ready™ approach to MIS Lapidus fusion. Englewood Cliffs, NJ – GLW, Inc. (“GLW Medical” or the “Company”), a medical technology company focused on orthopedic extremity and trauma surgery, today announced plans to preview the GLW Valerius™ Bunion Correction System at the American Orthopaedic Foot … Continued

GLW Medical Continues To Expand Its MIS Solutions, Introduces GLW Sabre™ MIS Bunion System

By orthoPro

GLW Sabre delivers a streamlined, instrumented workflow designed to support precise, reproducible percutaneous bunion correction. Englewood Cliffs, NJ – GLW, Inc. (“GLW Medical” or the “Company”), a medical technology company focused on advancing orthopedic extremity and trauma surgery, today announced a preview of its forthcoming GLW Sabre™ (the “System”) MIS bunion correction system, an innovative, … Continued

GLW Medical to Expand MIS Solutions and Introduce Creed Edge™ 

By orthoPro

Advancing foot & ankle MIS without compromise while preserving surgeon choice at every step. Englewood Cliffs, NJ – GLW, Inc. (“GLW Medical” or the “Company”), a medical technology company focused on advancing orthopedic extremity and trauma surgery, today announced its upcoming product showcase at the 2025 American Orthopaedic Foot & Ankle Society (AOFAS) Annual Meeting, taking … Continued

GLW Medical Announces Full Market Release of the Apollo AFX™ Ankle Fracture Plating System

By admin

Additive Manufactured. Hybrid Materials. 26 Plates. One Comprehensive Plating System. Englewood Cliffs, NJ., — GLW, Inc. (“GLW Medical” or the “Company”) with a focus on the foot and ankle orthopedic market is excited to announce the full market release of its Apollo Ankle Fracture (AFX) Plating System. The Company has commercialized its patented, first of … Continued

GLW Medical Announces Additional FDA 510(K) Clearance for the Artemis Proximal Femoral Nail System

By orthoPro

NEW LONG NAIL TO STRENGTHEN THE ARTEMIS PFN SYSTEM AND STREAMLINE WORKFLOWS Englewood Cliffs, NJ – GLW, Inc. (“GLW Medical” or the “Company”), a medical technology company focused on advancing orthopedic extremity and trauma surgery, today announced additional U.S. Food and Drug Administration (FDA) 510(k) clearance of the Artemis Proximal Femoral Long Nail (PFN) System, … Continued

GLW Medical Receives FDA 510(k) Clearance for Apollo AFX™ Ankle Fracture Plating System

By orthoPro

Englewood Cliffs, NJ – GLW, Inc. (“GLW Medical” or the “Company”), a medical technology company focused on advancing orthopedic extremity and trauma surgery, today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its upcoming Apollo Ankle Fracture (AFX) Plating System, a novel portfolio of see-through, “ortholucent” bone … Continued

Solvay and GLW Medical Partner on Creed™ Cannulated Compression Screws for Orthopedics

By orthoPro

Alpharetta, Ga., — Solvay’s Zeniva® polyetheretherketone (PEEK) resin was chosen by GLW, Inc (“GLW Medical”) 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 is … Continued

GLW Medical Announces FDA 510(K) Clearance for the Artemis Proximal Femoral Nail System

By admin

A FOURTH-GENERATION HIP FRACTURE NAIL MANUFACTURED USING A REVOLUTIONARY PROCESS Englewood Cliffs, NJ – GLW, Inc. (“GLW Medical” or the “Company”), a medical technology company focused on advancing orthopedic extremity and trauma surgery, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration for its Artemis Proximal Femoral Nail (PFN) … Continued

GLW Medical Receives FDA 510(k) Clearance for the Creed™ Cannulated Screw System

By admin

Englewood Cliffs, NJ – GLW, Inc. (“GLW Medical” or the “Company”), a medical technology company focused on advancing orthopedic extremity and trauma surgery, today announced that it has received 510(k) clearance from the U.S. Food & Drug Administration (FDA) to market the Creed™ Cannulated Screw System, a portfolio of unique, see-through “ortholucent” bone screws used … Continued

GLW Medical Receives FDA 510(k) Clearance for FusionFrame™ Ring Lock System

By admin

Carbon22 Consortium designed circular external fixator can treat complex foot and ankle deformities as well as provide a static frame for various indications. Englewood Cliffs, NJ – GLW, Inc. (“GLW Medical” or the “Company”), a medical technology company focused on advancing orthopedic extremity and trauma surgery, today announced that it has received 510(k) clearance from … Continued