Diorco Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Autolign Ref K192847
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diorco Co., Ltd. have in the registry?
The registry currently lists 3 devices for Diorco Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diorco Co., Ltd.'s devices?
Among its 3 most recently registered devices, Diorco Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Diorco Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Diorco Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diorco Co., Ltd. in the registry?
The most recently registered devices listed for Diorco Co., Ltd. include AUTOLIGN 1.0, DICAON 4D 1.0 and AUTOLIGN.