FDA device listing
LUMIFLEX 3-Stage Dilatation Balloon Catheter
FDA device listing 1850078922 · STERIS Corporation
Key facts
| Proprietary names | LUMIFLEX 3-Stage Dilatation Balloon Catheter |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 10078069 |
| Premarket submissions | K241888 |
| Product codes | FGE, KNQ |
| Device names | FGE - Stents, Drains And Dilators For The Biliary Ducts, KNQ - Dilator, Esophageal |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.5010, 876.5365 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | UNITED STATES ENDOSCOPY GROUP, INC. |
| Establishment registrations | 1528319 |
| FEI numbers | 1000122656 |
| Establishment operations | Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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