Hakko Shoji Co., Ltd.
Country not established
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Tuohy Epidural Needles Ref K961152
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Spinal Needles Ref K961151
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hakko Shoji Co., Ltd. have in the registry?
The registry currently lists 3 devices for Hakko Shoji Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hakko Shoji Co., Ltd.'s devices?
Among its 3 most recently registered devices, Hakko Shoji Co., Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Hakko Shoji Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Hakko Shoji Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hakko Shoji Co., Ltd. in the registry?
The most recently registered devices listed for Hakko Shoji Co., Ltd. include TUOHY EPIDURAL NEEDLES, LAP DISC 120 X 120MM X 2CM #LD111; LAP DISC 120 X 120MM X 7CM #LD112 and SPINAL NEEDLES.