Setagaya Seiki Co., Ltd.
Country not established FDA establishment FEI 3010388675
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
DIAMED Handpiece Ref K262144
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010388675
- Address
- 5-4862-11 Hachimanpara, Yonezawa-shi Yamagata
Frequently asked questions
How many devices does Setagaya Seiki Co., Ltd. have in the registry?
The registry currently lists 1 device for Setagaya Seiki Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Setagaya Seiki Co., Ltd.'s devices?
Among its 1 most recently registered device, Setagaya Seiki Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Setagaya Seiki Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Setagaya Seiki Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Setagaya Seiki Co., Ltd. in the registry?
The most recently registered devices listed for Setagaya Seiki Co., Ltd. include DIAMED Handpiece.