Dyna Flex is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dyna Flex - FDA 510(k) Cleared Devices
Recent clearances: DynaFlex Clear Brackets & Buttons, DynaFlex
4
Total
4
Cleared
0
Denied
Dyna Flex has 4 FDA 510(k) cleared medical devices. Based in Austin, US.
Last cleared in 2023. Active since 2011. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dyna Flex Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dyna Flex
4 devices