Glw, Inc. - FDA 510(k) Cleared Devices

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.