| EQS-News: Bendit Technologies / Key word(s): Miscellaneous/Product Launch TEL AVIV, Israel, Dec. 10, 2025 /PRNewswire/ -- Bendit Technologies is proud to announce that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the Bendit17™ Microcatheter, the smallest steerable microcatheter on the market. This milestone marks a significant step forward in advancing precision and accessibility in neurovascular and peripheral endovascular interventions.
The FDA clearance enables Bendit to bring its innovative technology to physicians and patients across the United States. The company is in the final stages of production and preparing to initiate its first U.S. commercial clinical procedures beginning in January 2026. In parallel, Bendit is actively pursuing additional regulatory clearances in other global territories. Oz Cabiri, CEO of Bendit Technologies, commented: The Bendit17 Microcatheter introduces a new level of steerability and precision, enabling controlled navigation through complex anatomies while maintaining stability, control, and ease of use. Its unique capabilities are designed to support clinicians across a broad range of intricate vascular procedures. About Bendit Technologies Photo - https://mma.prnewswire.com/media/2842527/Bendit_Technologies_Microcatheter.jpg Contact Details View original content:https://www.prnewswire.co.uk/news-releases/bendit-announces-fda-clearance-for-the-bendit17-steerable-microcatheter-302637745.html 10.12.2025 CET/CEST Dissemination of a Corporate News, transmitted by EQS News - a service of EQS Group. |
2243296 10.12.2025 CET/CEST