Eyedesigns Corp.
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What Eyedesigns Corp. makes
Eyedesigns Corp. manufactures spectacle frames and sunglasses designed for optical and protective eyewear applications. These products are intended for general use, including prescription and non-prescription eyewear.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where the company is based.
Catalogue
Spectacle Frames, Sunglasses Ref K936125
510(k) 510(k)
Frequently asked questions
How many devices does Eyedesigns Corp. have in the registry?
The registry currently lists 1 device for Eyedesigns Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eyedesigns Corp.'s devices?
Among its 1 most recently registered device, Eyedesigns Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Eyedesigns Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eyedesigns Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Eyedesigns Corp. in the registry?
The most recently registered devices listed for Eyedesigns Corp. include SPECTACLE FRAMES, SUNGLASSES.