FDA device listing
ENDO-MAGNIFIER,KARL STORZ ENDOSCOPE LENS
FDA device listing 1254083858 · KARL STORZ SE & CO KG
Key facts
| Proprietary names | ENDO-MAGNIFIER,KARL STORZ ENDOSCOPE LENS |
|---|---|
| Owner/operator | KARL STORZ SE & CO KG |
| Owner/operator number | 8010119 |
| Product codes | FEI |
| Device names | FEI - Instrument, Special Lens, For Endoscope |
| Device class | Class I |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Karl Storz Endoscopy-America, Inc., KARL STORZ ENDOSCOPY-AMERICA, INC. |
| Establishment registrations | 2020550, 3010202439 |
| FEI numbers | 2020550, 3007475226 |
| Establishment operations | Complaint File Establishment, Repackager/Relabeler |
| 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