FDA device listing
PROFORE WOUND CONTACT LAYER,TRICOTEX
FDA device listing 1172120991 · SMITH AND NEPHEW MEDICAL LTD.
Key facts
| Proprietary names | PROFORE WOUND CONTACT LAYER,TRICOTEX |
|---|---|
| Owner/operator | SMITH AND NEPHEW MEDICAL LTD. |
| Owner/operator number | 9001952 |
| Product codes | NAB |
| Device names | NAB - Gauze / Sponge,Nonresorbable For External Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4014 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Smith & Nephew Medical Ltd |
| Establishment registrations | 8043484 |
| FEI numbers | 3002808194 |
| Establishment operations | Specification Developer |
| 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