Tni Manufacturing, Inc. is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tni Manufacturing, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LONG SHEATH OR LS, 70 CM, LONG SHEATH OR LS, 80 CM, LONG SHEATH OR LS, 90 CM, Intermediate Catheter, 105 cm, Intermediate Catheter, 115cm, Intermediate Catheter , 125cm
2
Total
2
Cleared
0
Denied
Tni Manufacturing, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sunrise, US.
Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tni Manufacturing, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Inneuroco.
FDA 510(k) Regulatory Record - Tni Manufacturing, Inc.
2 devices