Sciara Intl., Inc.
Country not established
- Devices
- 1
What Sciara Intl., Inc. makes
Sciara Intl., Inc. manufactures spectacle frames, which are non-invasive optical devices designed to support eyeglasses for vision correction.
The company’s spectacle frames are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The products are based in the United States.
Catalogue
Spectacle Frame Ref K920170
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sciara Intl., Inc. have in the registry?
The registry currently lists 1 device for Sciara Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sciara Intl., Inc.'s devices?
Among its 1 most recently registered device, Sciara Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sciara Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sciara Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sciara Intl., Inc. in the registry?
The most recently registered devices listed for Sciara Intl., Inc. include SPECTACLE FRAME.