Ophthocare, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Ophthocare, Ltd. makes
Ophthocare, Ltd. manufactures the LCG (Liquid Crystal Glasses) System, a wearable optical device designed for vision correction and display integration.
The LCG System is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Lcg (Liquide Crystal Glasses) System Ref K050856
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ophthocare, Ltd. have in the registry?
The registry currently lists 1 device for Ophthocare, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ophthocare, Ltd.'s devices?
Among its 1 most recently registered device, Ophthocare, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ophthocare, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ophthocare, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ophthocare, Ltd. in the registry?
The most recently registered devices listed for Ophthocare, Ltd. include LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM.