Medical Device Manufacturer · US , Tempe , AZ

Medi-Globe Corporation - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006

Total

Cleared

Denied

Medi-Globe Corporation has 7 FDA 510(k) cleared medical devices. Based in Tempe, US.

Historical record: 7 cleared submissions from 2006 to 2016. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Medi-Globe Corporation Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

Medi-Globe Corporation is one of 15069 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medi-Globe Corporation

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 20, 2026