DreaMed Diabetes, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
DreaMed Diabetes, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: endo.digital Platform, Advisor Pro Platform, DreaMed Advisor Pro
5
Total
4
Cleared
1
Denied
DreaMed Diabetes, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Petah Tikva, Pob 3271, IL.
Last cleared in 2023. 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.
FDA 510(k) Regulatory Record - DreaMed Diabetes, Ltd.
5 devices