FDA device listing
Fighter™ Guidewire,Marvel™ Guidewire,Samurai™ Guidewire,Samurai™ RC Guidewire,Stretch Extension Wire
FDA device listing 1068623282 · FMD Co., Ltd.
Key facts
| Proprietary names | Fighter™ Guidewire,Marvel™ Guidewire,Samurai™ Guidewire,Samurai™ RC Guidewire,Stretch Extension Wire |
|---|---|
| Owner/operator | FMD Co., Ltd. |
| Owner/operator number | 10052039 |
| Premarket submissions | K151840 |
| Product codes | DQX |
| Device names | DQX - Wire, Guide, Catheter |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1330 |
| Review panels | Cardiovascular |
| Registered establishments | FMD. Co., Ltd., FMD Co., Ltd. Okinawa Factory |
| Establishment registrations | 3013023134, 3014977413 |
| FEI numbers | 3013023134, 3014977413 |
| Establishment operations | Contract Manufacturer, Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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