FDA device listing
Johnson & Johnson Vision Care
FDA device listing 1076814137 · Hood Container Corporation
Key facts
| Proprietary names | Johnson & Johnson Vision Care |
|---|---|
| Owner/operator | Hood Container Corporation |
| Owner/operator number | 9048058 |
| Premarket submissions | N18033 |
| Product codes | LPL, LPM |
| Device names | LPL - Lenses, Soft Contact, Daily Wear, LPM - Lenses, Soft Contact, Extended Wear |
| Device class | Class II, Class III |
| Classification regulations (21 CFR) | 886.5925 |
| Review panels | Ophthalmic |
| Registered establishments | HOOD CONTAINER CORPORATION |
| Establishment registrations | 1067084 |
| FEI numbers | 3003495738 |
| Establishment operations | Repackager/Relabeler |
| 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