Trice Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trice Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Tenex 2nd Generation System, mi-eye 3 needlescope with cannula, mi-tablet 3
3
Total
3
Cleared
0
Denied
Trice Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in King Of Prussia, US.
Latest FDA clearance: Nov 2024. Active since 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Trice Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trice Medical, Inc.
3 devices