FDA device listing
Clear View,Pro Control,SonoTip II,Vizeon
FDA device listing 1798346049 · MEDI-GLOBE GMBH
Key facts
| Proprietary names | Clear View,Pro Control,SonoTip II,Vizeon |
|---|---|
| Owner/operator | MEDI-GLOBE GMBH |
| Owner/operator number | 9011628 |
| Premarket submissions | K070129 |
| Product codes | FCG |
| Device names | FCG - Biopsy Needle |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1075 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | MEDI-GLOBE GMBH, MEDI-GLOBE SRO |
| Establishment registrations | 9680809, 3004129994, 3011146996 |
| FEI numbers | 3002995060, 3004129994, 3011146996 |
| Establishment operations | Contract Manufacturer, Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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