Viopti, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Viopti, Ltd. makes
Viopti, Ltd. manufactures the Polaroid ContactsPod, a device designed for the preparation and storage of contact lenses using a disposable, single-use pod system.
The Polaroid ContactsPod is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Polaroid Contactspod Ref K131783
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viopti, Ltd. have in the registry?
The registry currently lists 1 device for Viopti, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viopti, Ltd.'s devices?
Among its 1 most recently registered device, Viopti, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Viopti, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Viopti, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Viopti, Ltd. in the registry?
The most recently registered devices listed for Viopti, Ltd. include POLAROID CONTACTSPOD.