Medical Device Manufacturer · US , Roselle , IL

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

1 submissions · 1 cleared · Since 2021

Total

Cleared

Denied

Prodigident, Inc. has 1 FDA 510(k) cleared medical devices. Based in Roselle, US.

Last cleared in 2021. Active since 2021. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Prodigident, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Prodigident, Inc.

1 devices

1-1 of 1