Rex Implants, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rex Implants, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PiezoImplant System
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.
FDA 510(k) Regulatory Record - Rex Implants, Inc.
1 devices