Technidyne Corp.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Technidyne Corp. have in the registry?
The registry currently lists 2 devices for Technidyne Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technidyne Corp.'s devices?
Among its 2 most recently registered devices, Technidyne Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Technidyne Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Technidyne Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Technidyne Corp. in the registry?
The most recently registered devices listed for Technidyne Corp. include HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY and HEMOCHRON MODEL 8000/FACTOR VI PREMIER COAGULATION.