FDA device listing
DUODERM BANDAGE,DUODERM Original Patch (10 mm, 40 Count),DUODERM Original Patch (12 mm, 32 Count),DUODERM Original Patch…
FDA device listing 1628692952 · Jaywave Inc.
Key facts
| Proprietary names | DUODERM BANDAGE,DUODERM Original Patch (10 mm, 40 Count),DUODERM Original Patch (12 mm, 32 Count),DUODERM Original Patch (12 mm, 48 Count),DUODERM Original Patch (12 mm, 80 Count),DUODERM Overnight Patch (12 mm, 32 Count),DUODERM Overnight Patch (12 mm, 48 Count),DUODERM Overnight Patch (12 mm, 80 Count) |
|---|---|
| Owner/operator | Jaywave Inc. |
| Owner/operator number | 10095622 |
| Product codes | NAC |
| Device names | NAC - Dressing, Wound, Hydrophilic |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4018 |
| Review panels | General & Plastic Surgery |
| Registered establishments | JAYWAVE INC. |
| Establishment registrations | 3012387552 |
| FEI numbers | 3012387552 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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