FDA device listing
surgical adhesive dressing, surgical incise adhesive dressing, surgical incise adhesive film, surgical incise…
FDA device listing 1762867473 · Wuhan Hangu Technology Co.,Ltd
Key facts
| Proprietary names | surgical adhesive dressing, surgical incise adhesive dressing, surgical incise adhesive film, surgical incise dressing,,surgical incise film, surgical drape, surgical incise drape |
|---|---|
| Owner/operator | Wuhan Hangu Technology Co.,Ltd |
| Owner/operator number | 10094426 |
| Product codes | KGT |
| Device names | KGT - Drape, Adhesive, Aerosol |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4380 |
| Review panels | General & Plastic Surgery |
| Registered establishments | WUHAN HANGU TECHNOLOGY CO.,LTD |
| Establishment registrations | 3042277868 |
| FEI numbers | 3042277868 |
| Establishment operations | Contract Manufacturer, Foreign Exporter, 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