Eis Corporation
South KoreaFDA applicant, unverified
- Devices
- 1
What Eis Corporation makes
Eis Corporation manufactures pessaries, which are vaginal inserts used to support pelvic organs and treat conditions such as pelvic organ prolapse.
The company’s pessaries are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. Eis Corporation is based in the United States.
Catalogue
Pessary Ref K132313
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eis Corporation have in the registry?
The registry currently lists 1 device for Eis Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eis Corporation's devices?
Among its 1 most recently registered device, Eis Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Eis Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eis Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eis Corporation in the registry?
The most recently registered devices listed for Eis Corporation include PESSARY.