Medical Device Manufacturer · IL , Tel-Aviv

Medinol, Ltd. - FDA 510(k) Cleared Devices

6 submissions · 3 cleared · Since 1998

Total

Cleared

Denied

Medinol, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Tel-Aviv, IL.

Historical record: 3 cleared submissions from 1998 to 2018. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by Cardiomed Device Consultants as regulatory consultant.

Medinol, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medinol, Ltd.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Jun 08, 2026