Theranica Bioelectronics , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Theranica Bioelectronics , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: NerivioInfinity, Nerivio, Nerivio, FGD000075-4.7
4
Total
3
Cleared
1
Denied
Theranica Bioelectronics , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Netanya, IL.
Last cleared in 2023. Active since 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Theranica Bioelectronics , 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 - Theranica Bioelectronics , Ltd.
4 devices