FDA device listing
Medicom Ocean Pacific NeoNatural
FDA device listing 1789642177 · Medicom Group
Key facts
| Proprietary names | Medicom Ocean Pacific NeoNatural |
|---|---|
| Owner/operator | Medicom Group |
| Owner/operator number | 8020405 |
| Premarket submissions | K211758 |
| Product codes | LZC, OPC |
| Device names | LZC - Medical Glove, Specialty, OPC - Powder-Free Polychloroprene Patient Examination Glove |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6250 |
| Review panels | General Hospital |
| Registered establishments | AMD Medicom Inc. |
| Establishment registrations | 9611959 |
| FEI numbers | 3002677549 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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