Bend IT Technologies, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Bend IT Technologies, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Bendit17 Microcatheter, Bendit21 Microcatheter, Bendit2.7 Steerable Microcatheter
4
Total
4
Cleared
0
Denied
Bend IT Technologies, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Petach Tikva, IL.
Latest FDA clearance: Dec 2025. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Bend IT Technologies, Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Heyer Regulatory Solutions, LLC and Heyer Regulatory Solutions.
FDA 510(k) Regulatory Record - Bend IT Technologies, Ltd.
4 devices