Arno Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Arno Intl., Inc. makes
Arno Intl., Inc. manufactures optical devices, including frame spectacle lenses and contact lenses designed for vision correction.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Frame Spectacle Ref K934858
Regimes: 510(k) Registry: 510(k)Contact Lenses Ref K934859
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arno Intl., Inc. have in the registry?
The registry currently lists 2 devices for Arno Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arno Intl., Inc.'s devices?
Among its 2 most recently registered devices, Arno Intl., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Arno Intl., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arno Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Arno Intl., Inc. in the registry?
The most recently registered devices listed for Arno Intl., Inc. include FRAME SPECTACLE and CONTACT LENSES.