La Rue Optical
Country not established
- Devices
- 1
What La Rue Optical makes
La Rue Optical manufactures modified mydriatic spectacle lenses, designed to facilitate pupil dilation for diagnostic or procedural purposes in ophthalmology.
These devices are regulated under the FDA’s 510(k) pathway as Class II medical devices and are listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Modified Mydriatic Spectacle Ref K854140
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does La Rue Optical have in the registry?
The registry currently lists 1 device for La Rue Optical. Devices recorded under merged duplicate company entries are counted once.
Which registries list La Rue Optical's devices?
Among its 1 most recently registered device, La Rue Optical has devices listed in FDA 510(k) (1 device).
What are the newest devices from La Rue Optical in the registry?
The most recently registered devices listed for La Rue Optical include MODIFIED MYDRIATIC SPECTACLE.