Nike, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Nike, Inc. makes
Nike, Inc. manufactures MAGNETO EYEWEAR, a wearable device designed for augmented reality and fitness tracking, as well as NIKE V8 and NIKE V12, which appear to be smart athletic shoes with integrated sensors for performance monitoring and connectivity.
These devices are classified under Class I in regulatory frameworks, with the MAGNETO EYEWEAR and athletic shoes listed via FDA 510(k) clearance. The company is based in the United States.
Catalogue
Magneto Eyewear Ref K962169
510(k) 510(k)Nike V8 And Nike V12 Ref K962412
510(k) 510(k)
Frequently asked questions
How many devices does Nike, Inc. have in the registry?
The registry currently lists 2 devices for Nike, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nike, Inc.'s devices?
Among its 2 most recently registered devices, Nike, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nike, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nike, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nike, Inc. in the registry?
The most recently registered devices listed for Nike, Inc. include MAGNETO EYEWEAR and NIKE V8 AND NIKE V12.