Theranica Bio-Electronics, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Theranica Bio-Electronics, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Netanya, IL.
Latest FDA clearance: May 2025. Active since 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Theranica Bio-Electronics, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Theranica Bio-Electronics, Ltd.
3 devices