Medical Device Manufacturer · IL , Petah Tikva, Pob 3271

DreaMed Diabetes, Ltd. - FDA 510(k) Cleared Devices

6 submissions · 5 cleared · Since 2018

Total

Cleared

Denied

DreaMed Diabetes, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Petah Tikva, Pob 3271, IL.

Latest FDA clearance: Sep 2026. Active since 2018. Primary specialty: Chemistry.

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

1 device has linked clinical trial registered on ClinicalTrials.gov.

DreaMed Diabetes, Ltd. is one of 474 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - DreaMed Diabetes, Ltd.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Oct 05, 2026