Zilia, Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Zilia, Inc. makes
Zilia, Inc. manufactures the Zilia Ocular FC (ZIL-10002), a device designed for ocular applications, likely intended for corneal or anterior segment procedures.
The device falls under FDA Class II regulation and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Zilia Ocular FC (ZIL-10002) Ref K230627
510(k) 510(k)
Frequently asked questions
How many devices does Zilia, Inc. have in the registry?
The registry currently lists 1 device for Zilia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zilia, Inc.'s devices?
Among its 1 most recently registered device, Zilia, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Zilia, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Zilia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zilia, Inc. in the registry?
The most recently registered devices listed for Zilia, Inc. include Zilia Ocular FC (ZIL-10002).