FDA device listing
SDP HERNIA TAPE,SDP MESH GAUZE,SDP TWILL TAPE
FDA device listing 2059046436 · SDP Inc.
Key facts
| Proprietary names | SDP HERNIA TAPE,SDP MESH GAUZE,SDP TWILL TAPE |
|---|---|
| Owner/operator | SDP Inc. |
| Owner/operator number | 10052289 |
| Product codes | KGX |
| Device names | KGX - Tape And Bandage, Adhesive |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.5240 |
| Review panels | General Hospital |
| Registered establishments | SDP INC. |
| Establishment registrations | 3012660022 |
| FEI numbers | 3012660022 |
| Establishment operations | Complaint File Establishment, 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