Becker's Hospital Review

Renovis Surgical receives FDA clearance for first-ever 3D printed titanium stand-alone cervical cage

Renovis Surgical Technologies, Inc. today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the Tesera™ SC – Porous Titanium Cervical Interbody ...
Main Line

Centinel Spine(R) Announces First International Use of 3D-Printed Porous Titanium FLXTM Platform

WEST CHESTER, Pa., Sept. 14, 2021 /PRNewswire/ — Centinel Spine (R), LLC, a leading global medical device company addressing cervical and lumbar spinal disease through anterior surgical access, today ...
Becker's Hospital Review

Vertera cervical fusion device implanted for first time

Atlanta-based medical device developer Vertera Spine announced the first implantations of their Cohere Cervical Fusion Device, which features the company’s patented porous biomaterial technology. The ...
Healio

Window, non-window 3D-printed titanium cages had similar outcomes, interbody fusion rates

Please provide your email address to receive an email when new articles are posted on . Among 61 patients who underwent posterior lumbar interbody fusion, 95.1% achieved fusion. A non-window-type ...
Healio

ulrich Medical USA receives FDA 510(k) clearance of 3D-printed cervical interbody device

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. ulrich Medical USA Inc. has announced FDA 510(k) ...
KOIN 6

Curiteva Inc. Announces FDA 510(k) Clearance for Inspire 3D Porous PEEK HAFUSE Cervical Interbody System

HUNTSVILLE, Ala., Feb. 14, 2023 (GLOBE NEWSWIRE) -- Huntsville, Alabama-based technology company Curiteva announces the first FDA 510(k) cleared 3D-printed PEEK implant, the Inspire Porous PEEK ...