California Intraocular Lens
Country not established
- Devices
- 1
What California Intraocular Lens makes
California Intraocular Lens specializes in the CILCO Anterior Chamber Lens, a type of intraocular lens designed for implantation in the anterior chamber of the eye, typically used in cases where standard posterior chamber lenses are not suitable.
The company’s portfolio is regulated under FDA Class III designation, requiring premarket approval via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Cilco Anterior Chamber Lens Ref K771933
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does California Intraocular Lens have in the registry?
The registry currently lists 1 device for California Intraocular Lens. Devices recorded under merged duplicate company entries are counted once.
Which registries list California Intraocular Lens's devices?
Among its 1 most recently registered device, California Intraocular Lens has devices listed in FDA 510(k) (1 device).
What risk classes do California Intraocular Lens's devices fall under?
Among its 1 most recently registered device, the classes recorded for California Intraocular Lens's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from California Intraocular Lens in the registry?
The most recently registered devices listed for California Intraocular Lens include CILCO ANTERIOR CHAMBER LENS.