Rex Implants, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Rex Implants, Inc. has 1 FDA 510(k) cleared medical devices. Based in Columbus, US.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Rex Implants, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Backroads Consulting as regulatory consultant.
1 devices