G-Medical Innovations , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
G-Medical Innovations , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Prizma
2
Total
2
Cleared
0
Denied
G-Medical Innovations , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Rehovot, IL.
Historical record: 2 cleared submissions from 2017 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by G-Medical Innovations , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - G-Medical Innovations , Ltd.
2 devices