FDA device listing
TriClip G4 Clip Delivery System,TriClip G5 Delivery System,TriClip NTR Clip Delivery System,TriClip XTR Clip Delivery…
FDA device listing 1750365230 · ABBOTT LABORATORIES
Key facts
| Proprietary names | TriClip G4 Clip Delivery System,TriClip G5 Delivery System,TriClip NTR Clip Delivery System,TriClip XTR Clip Delivery System |
|---|---|
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| Product codes | NPS |
| Device names | NPS - Tricuspid Valve Repair Device, Percutaneously Delivered |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.NPS |
| Review panels | Cardiovascular |
| Registered establishments | Abbott Vascular |
| Establishment registrations | 3005070406 |
| FEI numbers | 3005070406 |
| Establishment operations | U.S. Manufacturer of Export Only Devices |
| 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