Triad Surgical Technologies, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Triad Surgical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MOD
1
Total
1
Cleared
0
Denied
Triad Surgical Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Triad Surgical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Triad Surgical Technologies, Inc.
1 devices