Kera Corp.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Kerascan Model 2000 Keratographic Auto Analyzer Ref K864037
Regimes: 510(k) Registry: 510(k)Corneascope Model 1200 Ref K850665
Regimes: 510(k) Registry: 510(k)Videoscan (Tm) Ref K871479
Regimes: 510(k) Registry: 510(k)Model 2000 Intraoperative Corneascope Ref K901009
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kera Corp. have in the registry?
The registry currently lists 4 devices for Kera Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kera Corp.'s devices?
Among its 4 most recently registered devices, Kera Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Kera Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Kera Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kera Corp. in the registry?
The most recently registered devices listed for Kera Corp. include KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZER, CORNEASCOPE MODEL 1200, VIDEOSCAN (TM) and MODEL 2000 INTRAOPERATIVE CORNEASCOPE.