Eyeworks 3
Country not established
- Devices
- 2
What Eyeworks 3 makes
Eyeworks 3 manufactures non-prescription sunglasses and spectacle frames, including plastic and metal designs, intended for general eye protection and fashion use.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does Eyeworks 3 have in the registry?
The registry currently lists 2 devices for Eyeworks 3. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eyeworks 3's devices?
Among its 2 most recently registered devices, Eyeworks 3 has devices listed in FDA 510(k) (2 devices).
What risk classes do Eyeworks 3's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eyeworks 3's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Eyeworks 3 in the registry?
The most recently registered devices listed for Eyeworks 3 include THEO NON-PRESCRIPTION SUNGLASSES/SPECTACLE FRAMES and NON-PRES SUNGLASSES/SPEC FRAMES (PLASTIC & METAL).