Benson & Ashley, Inc.
Country not established
- Devices
- 1
What Benson & Ashley, Inc. makes
Benson & Ashley, Inc. manufactures Class I medical devices, including the Benson and Ashley brand of products, which are designed for specific clinical applications in the healthcare setting.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, with devices listed in the US regulatory system. The manufacturer is based in the United States.
Catalogue
Benson And Ashley Ref K951438
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Benson & Ashley, Inc. have in the registry?
The registry currently lists 1 device for Benson & Ashley, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Benson & Ashley, Inc.'s devices?
Among its 1 most recently registered device, Benson & Ashley, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Benson & Ashley, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Benson & Ashley, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Benson & Ashley, Inc. in the registry?
The most recently registered devices listed for Benson & Ashley, Inc. include BENSON AND ASHLEY.