Beshape Technologies , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Beshape Technologies , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: BeShape One™ Device
1
Total
1
Cleared
0
Denied
Beshape Technologies , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Kfar-Saba, IL.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Beshape Technologies , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by A. Stein – Regulatory Affairs Consulting , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Beshape Technologies , Ltd.
1 devices