Elminda, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Elminda, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: BNA Platform
1
Total
1
Cleared
0
Denied
Elminda, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Herzliya, IL.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Elminda, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biologics Consulting as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Elminda, Ltd.
1 devices