FDA device listing
Sealing caps,Three slot membrane,Uretero-Renoscope
FDA device listing 1966746339 · SCHOELLY FIBEROPTIC, GMBH
Key facts
| Proprietary names | Sealing caps,Three slot membrane,Uretero-Renoscope |
|---|---|
| Owner/operator | SCHOELLY FIBEROPTIC, GMBH |
| Owner/operator number | 9004385 |
| Premarket submissions | K992527 |
| Product codes | FGB |
| Device names | FGB - Ureteroscope And Accessories, Flexible/Rigid |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | SCHOELLY FIBEROPTIC, GMBH, SCHOELLY-OPTIX OOD |
| Establishment registrations | 8043903, 3014644276 |
| FEI numbers | 3002808088, 3006149253 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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