FDA device listing
Color Cuff Cylindrical Tourniquet,Color Cuff Disposable Tourniquet,ExpressAire Tourniquet Cuff,Tourniquet Cuff
FDA device listing 1866885679 · Medline Industries, LP
Key facts
| Proprietary names | Color Cuff Cylindrical Tourniquet,Color Cuff Disposable Tourniquet,ExpressAire Tourniquet Cuff,Tourniquet Cuff |
|---|---|
| Owner/operator | Medline Industries, LP |
| Owner/operator number | 1417592 |
| Product codes | KCY |
| Device names | KCY - Tourniquet, Pneumatic |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.5910 |
| Review panels | General & Plastic Surgery |
| Registered establishments | MEDLINE INDUSTRIES, LP (Northpoint Services) |
| Establishment registrations | 1422634 |
| FEI numbers | 1000514656 |
| Establishment operations | Contract Sterilizer |
| 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