Triad Life Sciences, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Triad Life Sciences, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InnovaBurn, InnovaMatrix PD, InnovaMatrix FS
4
Total
4
Cleared
0
Denied
Triad Life Sciences, Inc. has 4 FDA 510(k) cleared medical devices. Based in Memphis, US.
Last cleared in 2022. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Triad Life Sciences, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Streamline Regulatory as regulatory consultant.
FDA 510(k) Regulatory Record - Triad Life Sciences, Inc.
4 devices