FDA device listing
Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia
FDA device listing 1568709990 · COOPERVISION, INC.
Key facts
| Owner/operator | COOPERVISION, INC. |
|---|---|
| Owner/operator number | 9929062 |
| Premarket submissions | P180035 |
| Product codes | QIT |
| Device names | QIT - Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.QIT |
| Review panels | Ophthalmic |
| Registered establishments | CooperVision, Inc., COOPERVISION INC., CooperVision Limited, CooperVision Manufacturing, LTD., COOPERVISION MANUFACTURING, LTD. |
| Establishment registrations | 9614374, 3003981983, 3005724763, 3008586477, 3011771819 |
| FEI numbers | 3002807783, 3003981983, 3005724763, 3008586477, 3011771819 |
| Establishment operations | Complaint File Establishment, Manufacturer, Repackager/Relabeler, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 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