Endospan Ltd
Active in EUDAMEDIsraelfrom SRN EUDAMED FDA SRN IL-MF-000014169 FEI 3009304068
- Devices
- 132
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
2 of 2 in force.
Market reach
- European Union
- EUDAMED actor, 2 certificates
- United States
- FDA FEI
What Endospan Ltd makes
Endospan, Ltd. manufactures the NEXUS Aortic Arch Stent Graft System, a device designed for endovascular repair of aortic arch aneurysms and complex aortic pathologies. The system is intended to provide structural support and exclude blood flow from the aneurysm sac while maintaining patency of the true lumen.
The NEXUS Aortic Arch Stent Graft System is classified as a Class III medical device under FDA regulations and is listed under a Premarket Approval (PMA) application. The company is based in the United States.
Catalogue
Search and filter all 132 devicesShowing 1-50 of 132
Company details
- EUDAMED SRN
- IL-MF-000014169
- FDA FEI number
- 3009304068
- DUNS number
- 532700825
- EUDAMED status
- Active
- EUDAMED registered name
- Endospan Ltd
- Registered address
- 4, Maskit St., 4673304, Herzliya, Israel
- Website
- www.endospan.com/
- [email protected]
- Phone
- +972-9-7884620
- PRRC contact
- Shiran Mor Yossef
EUDAMED certificates
2 certificates2 valid, 0 expiredMDR 2next expiry 11 Feb 2031
TÜV SÜD Product Service GmbH 0123 2 certificates
- G70 132171 0004 Active
Technical documentation EU MDR
- Issued
- 12 Oct 2026
- Expires
- 23 Jun 2031
- Reason
- Add device or group
- G15 132171 0003 Active
Quality management system EU MDR
- Issued
- 30 Jul 2026
- Expires
- 11 Feb 2031
- Reason
- Add device or group
Frequently asked questions
How many devices does Endospan Ltd have in the registry?
The registry currently lists 132 devices for Endospan Ltd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endospan Ltd's devices?
Among its 50 most recently registered devices, Endospan Ltd has devices listed in EUDAMED (50 devices).
What risk classes do Endospan Ltd's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Endospan Ltd's devices are Class III. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Endospan Ltd?
EUDAMED lists 2 certificates for Endospan Ltd (technical documentation; quality management system) under MDR. The most recent was issued on 12 Oct 2026.
What are the newest devices from Endospan Ltd in the registry?
The most recently registered devices listed for Endospan Ltd include NEXUS.