Plexus Optix, Inc.
United Statesfrom the FDA registration address FDA FEI 3011503801
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Plexus Optix, Inc. makes
Plexus Optix, Inc. manufactures Ethos Aquell (Hioxifilcon A) one-day soft contact lenses with a 59% water content, designed for daily disposable use.
The company’s portfolio is regulated under FDA Class II devices and listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3011503801
- Address
- 11135 Trade Center Dr Ste 130, Rancho Cordova, CA, 95670
Frequently asked questions
How many devices does Plexus Optix, Inc. have in the registry?
The registry currently lists 1 device for Plexus Optix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Plexus Optix, Inc.'s devices?
Among its 1 most recently registered device, Plexus Optix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Plexus Optix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Plexus Optix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Plexus Optix, Inc. in the registry?
The most recently registered devices listed for Plexus Optix, Inc. include Ethos Aquell (Hioxifilcon A) One-Day Soft (Hydrophilic) Contact Lenses (59% Water).