Skia, Inc.
South KoreaFDA applicant, unverified
- Devices
- 1
What Skia, Inc. makes
Skia, Inc. manufactures the SKIA-Head (Model SKIA-ST00), a medical device designed for monitoring and recording head movement or positioning in clinical or research settings.
The SKIA-Head is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
SKIA-Head (Model: SKIA-ST00) Ref K253486
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Skia, Inc. have in the registry?
The registry currently lists 1 device for Skia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Skia, Inc.'s devices?
Among its 1 most recently registered device, Skia, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Skia, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Skia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Skia, Inc. in the registry?
The most recently registered devices listed for Skia, Inc. include SKIA-Head (Model: SKIA-ST00).