Medical Device Manufacturer · US , Grayslake , IL

Radius Intl., Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Radius Intl., Inc. has 5 FDA 510(k) cleared medical devices. Based in Grayslake, US.

Historical record: 5 cleared submissions from 1995 to 1998. Primary specialty: Gastroenterology & Urology.

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

Radius Intl., Inc. 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 - Radius Intl., Inc.

5 devices

1-5 of 5