Glw, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Glw, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CREED™ Cannulated Screws, Artemis Proximal Femoral Nail System, Artemis Proximal Femoral Nail System
3
Total
3
Cleared
0
Denied
Glw, Inc. has 3 FDA 510(k) cleared medical devices. Based in Englewood Cliff, US.
Last cleared in 2023. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Glw, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Wagoner Consulting, LLC and Lincé Consulting, LLC.
FDA 510(k) Regulatory Record - Glw, Inc.
3 devices