Targus Concepts
Country not established
- Devices
- 1
What Targus Concepts makes
Targus Concepts manufactures the Model Biostar, a Class II medical device designed for use in surgical procedures, likely as a sterile drape or barrier system to maintain a controlled environment during operations.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the U.S. regulatory database. The manufacturer is based in the United States.
Catalogue
Model Biostar Ref K882062
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Targus Concepts have in the registry?
The registry currently lists 1 device for Targus Concepts. Devices recorded under merged duplicate company entries are counted once.
Which registries list Targus Concepts's devices?
Among its 1 most recently registered device, Targus Concepts has devices listed in FDA 510(k) (1 device).
What risk classes do Targus Concepts's devices fall under?
Among its 1 most recently registered device, the classes recorded for Targus Concepts's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Targus Concepts in the registry?
The most recently registered devices listed for Targus Concepts include MODEL BIOSTAR.