Ecleris USA
Country not established
- Devices
- 2
What Ecleris USA makes
Ecleris USA makes the Ecleris Sinuscope and the Ecleris Microstar Colposcope.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ecleris Sinuscope Ref K131323
Regimes: 510(k) Registry: 510(k)Ecleris Microstar Colposcope Ref K100595
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ecleris USA have in the registry?
The registry currently lists 2 devices for Ecleris USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ecleris USA's devices?
Among its 2 most recently registered devices, Ecleris USA has devices listed in FDA 510(k) (2 devices).
What risk classes do Ecleris USA's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ecleris USA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ecleris USA in the registry?
The most recently registered devices listed for Ecleris USA include ECLERIS SINUSCOPE and ECLERIS MICROSTAR COLPOSCOPE.