Tribofilm Research, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tribofilm Research, Inc. - FDA 510(k) Cleared Devices
Recent clearances: StaClear Syringe
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.
510(k) submissions have been managed by Namsa as regulatory consultant.
FDA 510(k) Regulatory Record - Tribofilm Research, Inc.
2 devices