Accellent, Inc.
Country not established
- Devices
- 1
What Accellent, Inc. makes
Accellent, Inc. manufactures guidewires, including models such as the G-V220-3527S and others, designed for use in interventional procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Guidewire, Model G-V220-3527S And Others Ref K072354
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Accellent, Inc. have in the registry?
The registry currently lists 1 device for Accellent, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Accellent, Inc.'s devices?
Among its 1 most recently registered device, Accellent, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Accellent, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Accellent, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Accellent, Inc. in the registry?
The most recently registered devices listed for Accellent, Inc. include GUIDEWIRE, MODEL G-V220-3527S AND OTHERS.