New Brillette A/S
DenmarkFDA applicant, unverified
- Devices
- 1
What New Brillette A/S makes
New Brillette A/S manufactures spectacle frames, which are designed for optical correction and eyewear support.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Spectacle Frame Ref K851130
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New Brillette A/S have in the registry?
The registry currently lists 1 device for New Brillette A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list New Brillette A/S's devices?
Among its 1 most recently registered device, New Brillette A/S has devices listed in FDA 510(k) (1 device).
What risk classes do New Brillette A/S's devices fall under?
Among its 1 most recently registered device, the classes recorded for New Brillette A/S's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from New Brillette A/S in the registry?
The most recently registered devices listed for New Brillette A/S include SPECTACLE FRAME.