Endarx, Inc.
Country not established
- Devices
- 1
What Endarx, Inc. makes
Endarx, Inc. manufactures the ENDOHELIX ENDARTERECTOMY DEVICE, a specialized instrument used to perform endarterectomy procedures.
The device is classified as Class II and is listed in the FDA 510(k) registry. Endarx is based in the United States.
Catalogue
Endohelix Endarterectomy Device Ref K032105
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endarx, Inc. have in the registry?
The registry currently lists 1 device for Endarx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endarx, Inc.'s devices?
Among its 1 most recently registered device, Endarx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Endarx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Endarx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endarx, Inc. in the registry?
The most recently registered devices listed for Endarx, Inc. include ENDOHELIX ENDARTERECTOMY DEVICE.