Shannon Group
Country not established
- Devices
- 2
What Shannon Group makes
The Shannon Group manufactures an electro surgical cautery pencil for tissue sealing and cutting procedures, as well as molded polysulfone trial prostheses designed for temporary or test fitting in surgical applications.
Their devices are regulated under FDA Class I and Class II classifications, with authorisation via the 510(k) pathway. The company is based in the United States.
Catalogue
Their Electro Surgical Coutery Pencil Ref K820156
Regimes: 510(k) Registry: 510(k)Molded Polysulfone Trial Prosthesis Ref K811205
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shannon Group have in the registry?
The registry currently lists 2 devices for Shannon Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shannon Group's devices?
Among its 2 most recently registered devices, Shannon Group has devices listed in FDA 510(k) (2 devices).
What risk classes do Shannon Group's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Shannon Group's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shannon Group in the registry?
The most recently registered devices listed for Shannon Group include THEIR ELECTRO SURGICAL COUTERY PENCIL and MOLDED POLYSULFONE TRIAL PROSTHESIS.