FDA device listing
LOFTUS 2-Level ACDF Distractor,Septal Hook - Retractor
FDA device listing 1095386593 · Berger Surgical Medical Products GmbH
Key facts
| Proprietary names | LOFTUS 2-Level ACDF Distractor,Septal Hook - Retractor |
|---|---|
| Owner/operator | Berger Surgical Medical Products GmbH |
| Owner/operator number | 10055726 |
| Product codes | GAD |
| Device names | GAD - Retractor |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Berger Surgical Medical Products GmbH |
| Establishment registrations | 3013784566 |
| FEI numbers | 3013784566 |
| Establishment operations | Contract Manufacturer, Manufacturer, Remanufacturer |
| 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