Biobeat Technologies , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Biobeat Technologies , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: BB-613-BPM, Biobeat Platform-2 and BB-613WP Patch, Biobeat Platform, BB-613WP Patch
4
Total
4
Cleared
0
Denied
Biobeat Technologies , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Petah Tikvah, IL.
Latest FDA clearance: Jan 2025. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Biobeat Technologies , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and Hogan Lovells US Lpp. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Biobeat Technologies , Ltd.
4 devices