Endo Optics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Endo Optiks Value Pack Ref K923600
Regimes: 510(k) Registry: 510(k)The Endo Optiks Microprobe Ref K924090
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endo Optics, Inc. have in the registry?
The registry currently lists 2 devices for Endo Optics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endo Optics, Inc.'s devices?
Among its 2 most recently registered devices, Endo Optics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Endo Optics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Endo Optics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endo Optics, Inc. in the registry?
The most recently registered devices listed for Endo Optics, Inc. include ENDO OPTIKS VALUE PACK and THE ENDO OPTIKS MICROPROBE.