FDA device listing
Reusable Clip Removers HRK-LXL,Reusable Clip Removers HRK-MLL,Reusable Clip Removers HRK-MML,Reusable Clip Removers…
FDA device listing 1919248561 · Fengh Medical Co., Ltd.
Key facts
| Proprietary names | Reusable Clip Removers HRK-LXL,Reusable Clip Removers HRK-MLL,Reusable Clip Removers HRK-MML,Reusable Clip Removers HRQ-LXL,Reusable Clip Removers HRQ-MLL,Reusable Clip Removers HRQ-MML |
|---|---|
| Owner/operator | Fengh Medical Co., Ltd. |
| Owner/operator number | 10061944 |
| Product codes | HBQ |
| Device names | HBQ - Instrument, Clip Removal |
| Device class | Class I |
| Classification regulations (21 CFR) | 882.4200 |
| Review panels | Neurology |
| Registered establishments | FENGH MEDICAL CO., LTD. |
| Establishment registrations | 3011052945 |
| FEI numbers | 3011052945 |
| 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