Triowave Technologies is one of 22612 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Triowave Technologies - FDA 510(k) Cleared Devices
Recent clearances: PainKARE
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.
510(k) submissions have been managed by Elexes, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Triowave Technologies
1 devices