FDA device listing
Power LED 175
FDA device listing 1581238642 · KARL STORZ SE & CO KG
Key facts
| Proprietary names | Power LED 175 |
|---|---|
| Owner/operator | KARL STORZ SE & CO KG |
| Owner/operator number | 8010119 |
| Premarket submissions | K123956 |
| Product codes | FCW, NTN |
| Device names | FCW - Light Source, Fiberoptic, Routine, NTN - Led Light Source |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Karl Storz Endoscopy-America, Inc., KARL STORZ ENDOSCOPY-AMERICA, INC., KARL STORZ SE & CO KG, KARL STORZ SE & CO. KG |
| Establishment registrations | 2020550, 9610617, 3010202439, 3014342096 |
| FEI numbers | 2020550, 3002808268, 3007475226, 3014342096 |
| Establishment operations | Complaint File Establishment, Contract Manufacturer, Repackager/Relabeler, Specification Developer |
| 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