Data / Medical devices / Israel / Bend It Technologies Ltd.
Bend It Technologies Ltd.: FDA-registered device maker in Petach Tikva Central, Israel, 2 510(k) clearances
Bend It Technologies Ltd. is registered with the FDA (registration 3017278832) in Petach Tikva Central, Israel. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 3, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017278832
- Address
- 25 Basel Street, Petach Tikva Central, Israel, 4951038
- Owner or operator
- Bend It Technologies LTD. (10077053)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- April 18, 2022
- Registered through
- 2026
- Brand names listed
- Bendit17 Microcatheter, Bendit21 Microcatheter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Percutaneous | DQY | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Catheter, Percutaneous, Neurovasculature | QJP | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 3, 2025 | K252213 | Bendit17 Microcatheter | QJP | Substantially Equivalent | Bend IT Technologies, Ltd. | accessdata.fda.gov |
| April 13, 2022 | K203842 | Bendit21 Microcatheter | QJP | Substantially Equivalent | Bend IT Technologies, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 3, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.