Data / Medical devices / Israel / Endospan Ltd
Endospan Ltd: FDA-registered device maker in Herzliya Central, Israel, 1 PMA approval
Endospan Ltd is registered with the FDA (registration 3009304068) in Herzliya Central, Israel. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated April 2, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009304068
- Address
- 4 Maskit St, Herzliya Central, Israel, 4673304
- Owner or operator
- Endospan (10095741)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- April 22, 2026
- Registered through
- 2026
- Brand names listed
- NEXUS Aortic Arch Stent Graft System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Endovascular System For Treatment Of Ascending Aorta And Aortic Arch Lesions | SDZ | 3 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| April 2, 2026 | P250033 | NEXUS Aortic Arch Stent Graft System | SDZ | 3 | September 21, 2026 | accessdata.fda.gov |
Updated September 21, 2026. 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.