Dinona Co., Ltd.
Country not established
- Devices
- 1
What Dinona Co., Ltd. makes
Dinona Co., Ltd. manufactures the SELLAS, a medical device designed for targeted tissue ablation or treatment procedures.
The SELLAS device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Sellas Ref K080382
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dinona Co., Ltd. have in the registry?
The registry currently lists 1 device for Dinona Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dinona Co., Ltd.'s devices?
Among its 1 most recently registered device, Dinona Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dinona Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dinona Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dinona Co., Ltd. in the registry?
The most recently registered devices listed for Dinona Co., Ltd. include SELLAS.