Aristar Inc. U.S.A.
Country not established
- Devices
- 2
What Aristar Inc. U.S.A. makes
Aristar Inc. manufactures ARISTAR EYEWEAR and ESPRIT EYEWEAR, which are designed as corrective or protective eyewear for medical or clinical use.
These devices are classified as Class I under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Aristar Eyewear, Esprit Eyewear Ref K945123
Regimes: 510(k) Registry: 510(k)Aristar Eyewear, Esprit Eyewear Ref K945122
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aristar Inc. U.S.A. have in the registry?
The registry currently lists 2 devices for Aristar Inc. U.S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aristar Inc. U.S.A.'s devices?
Among its 2 most recently registered devices, Aristar Inc. U.S.A. has devices listed in FDA 510(k) (2 devices).
What risk classes do Aristar Inc. U.S.A.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aristar Inc. U.S.A.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Aristar Inc. U.S.A. in the registry?
The most recently registered devices listed for Aristar Inc. U.S.A. include ARISTAR EYEWEAR, ESPRIT EYEWEAR.