Glw Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Glw Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Apollo Ankle Fracture Plating System, CREED™ Cannulated Screws
2
Total
2
Cleared
0
Denied
Glw Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Englewood Cliff, US.
Last cleared in 2022. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Glw Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wagoner Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Glw Medical, Inc.
2 devices