Tribofilm Research, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Tribofilm Research, Inc. has 2 FDA 510(k) cleared medical devices. Based in Raleigh, US.
Historical record: 2 cleared submissions from 2007 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tribofilm Research, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Tribofilm Research, Inc.
2 devices