Accogent, LLC
Country not established
- Devices
- 1
What Accogent, LLC makes
Accogent, LLC manufactures the BLADEVIEW, a device designed for visualizing and enhancing surgical precision during procedures involving blades or sharp instruments.
The BLADEVIEW is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Bladeview Ref K101042
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Accogent, LLC have in the registry?
The registry currently lists 1 device for Accogent, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Accogent, LLC's devices?
Among its 1 most recently registered device, Accogent, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Accogent, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Accogent, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Accogent, LLC in the registry?
The most recently registered devices listed for Accogent, LLC include BLADEVIEW.