FDA device listing
Clariti 1 Day,Clariti 1 Day Multifocal,Clariti 1 Day Toric
FDA device listing 1183405081 · COOPERVISION, INC.
Key facts
| Proprietary names | Clariti 1 Day,Clariti 1 Day Multifocal,Clariti 1 Day Toric |
|---|---|
| Owner/operator | COOPERVISION, INC. |
| Owner/operator number | 9929062 |
| Premarket submissions | K181920 |
| Product codes | LPL, MVN |
| Device names | LPL - Lenses, Soft Contact, Daily Wear, MVN - Lens, Contact, (Disposable) |
| Device class | Class II |
| Classification regulations (21 CFR) | 886.5925 |
| Review panels | Ophthalmic |
| Registered establishments | CooperVision CL KFT, CooperVision, Inc., COOPERVISION INC., CooperVision Manufacturing Costa Rica SRL, CooperVision Manufacturing Ltd, CooperVision Manufacturing, LTD. |
| Establishment registrations | 3005724763, 3006514242, 3008586477, 3009108089, 3011771819, 3012123291 |
| FEI numbers | 3005724763, 3006514242, 3008586477, 3009108089, 3011771819, 3012123291 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Manufacturer, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 10–99 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database