Medical Device Manufacturer · US , Cliffside Park , NJ

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

7 submissions · 7 cleared · Since 1996

Total

Cleared

Denied

Gallini Intl., Inc. has 7 FDA 510(k) cleared medical devices. Based in Cliffside Park, US.

Historical record: 7 cleared submissions from 1996 to 1997. Primary specialty: Gastroenterology & Urology.

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

Gallini 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 - Gallini Intl., Inc.

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026