Endovascular Engineering Inc.
Active in EUDAMEDUnited Statesfrom EUDAMED address EUDAMED FDA SRN US-MF-000057846
- Devices
- 5
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA establishment
Catalogue
- GUDID
- GUDID
- GUDID
Helo™ Return Ref K253717
510(k) 510(k)Helo Max Thrombectomy System (HEL2090) Ref K261800
510(k) 510(k)
Company details
- EUDAMED SRN
- US-MF-000057846
- DUNS number
- 117560059
- EUDAMED status
- Active
- EUDAMED registered name
- Endovascular Engineering Inc.
- [email protected]
- PRRC contact
- Debra Cogan
FDA establishments
- Endovascular Engineering, Inc. Menlo Park, CA · US FEI 3026567963
Frequently asked questions
How many devices does Endovascular Engineering Inc. have in the registry?
The registry currently lists 5 devices for Endovascular Engineering Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endovascular Engineering Inc.'s devices?
Among its 5 most recently registered devices, Endovascular Engineering Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Endovascular Engineering Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Endovascular Engineering Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endovascular Engineering Inc. in the registry?
The most recently registered devices listed for Endovascular Engineering Inc. include Helo Max Thrombectomy System HEL2090, Helo Thrombectomy System HEL1595, Helo G1 Thrombectomy System 20001 and Helo™ Return.
Which FDA establishments are linked to Endovascular Engineering Inc.?
1 FDA establishment is linked to Endovascular Engineering Inc. in the registry; they are listed on the company page.