Triowave Technologies is one of 4891 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Triowave Technologies - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Triowave Technologies has 1 FDA 510(k) cleared medical devices. Based in Fremont, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Triowave Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Triowave Technologies
1 devices