Neteera Technologies , Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Neteera Technologies , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Jerusalem, IL.
Latest FDA clearance: Feb 2024. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Neteera Technologies , 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.
2 devices