Medical Device Manufacturer · US , Clinton , TN

Dyna Flex, Intl. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1990

Total

Cleared

Denied

Dyna Flex, Intl. has 4 FDA 510(k) cleared medical devices. Based in Clinton, US.

Historical record: 4 cleared submissions from 1990 to 1991. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Dyna Flex, Intl. Filter by specialty or product code using the sidebar.

Dyna Flex, Intl. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dyna Flex, Intl.

4 devices

1-4 of 4