FDA device listing
AED Brow Lift Retractor,AED BURKE GYN Forceps,AED Flexible Biopsy Cup,AED Flexible Forceps,AED Flexible Grasper,AED…
FDA device listing 1917215576 · NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
Key facts
| Proprietary names | AED Brow Lift Retractor,AED BURKE GYN Forceps,AED Flexible Biopsy Cup,AED Flexible Forceps,AED Flexible Grasper,AED Flexible Scissor,AED Rigid Optical Cup,AED Rigid Optical Forceps,AED TISHLER-BABY GYN Forceps,AED TISHLER-MORGAN GYN Forceps |
|---|---|
| Owner/operator | NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. |
| Owner/operator number | 9027397 |
| Product codes | GEN |
| Device names | GEN - Forceps, General & Plastic Surgery |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. |
| Establishment registrations | 2085947 |
| FEI numbers | 3000204191 |
| Establishment operations | Manufacturer |
| 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