Artegraft, Inc.
Country not established
- Devices
- 1
What Artegraft, Inc. makes
Artegraft, Inc. manufactures the D-CLOT Thrombectomy Catheter System (Model DC 4006), a device designed for the mechanical removal of thrombi within blood vessels, including coronary arteries.
The company’s portfolio is regulated under FDA’s Class II device classification, with the D-CLOT system authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Artegraft, Inc. have in the registry?
The registry currently lists 1 device for Artegraft, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artegraft, Inc.'s devices?
Among its 1 most recently registered device, Artegraft, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Artegraft, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Artegraft, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artegraft, Inc. in the registry?
The most recently registered devices listed for Artegraft, Inc. include D-CLOT THROMBECTOMY CATHETER SYSTEM, MODEL: DC 4006.