American Contact Lens, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What American Contact Lens, Inc. makes
American Contact Lens, Inc. manufactures spherical and toric soft contact lenses designed for daily wear, including clear and blue visibility-handling variants. These lenses are made from methafilcon A and hi-oxifilcon A materials and are intended for vision correction.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Biocurve Soft (Methafilcon A) Spherical And Toric Soft Contact Lens For Daily Wear (Clear, Lathe-Cut) Ref K010223
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Contact Lens, Inc. have in the registry?
The registry currently lists 2 devices for American Contact Lens, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Contact Lens, Inc.'s devices?
Among its 2 most recently registered devices, American Contact Lens, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do American Contact Lens, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for American Contact Lens, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Contact Lens, Inc. in the registry?
The most recently registered devices listed for American Contact Lens, Inc. include BIOCURVE SOFT (METHAFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT) and BIOCURVE SOFT (HIOXIFILCOM A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND BLUE VISIBILITY-HANDLING T.