FDA device listing
HNM Medical Surgical Instrument
FDA device listing 1386383577 · HNM Medical
Key facts
| Proprietary names | HNM Medical Surgical Instrument |
|---|---|
| Owner/operator | HNM Medical |
| Owner/operator number | 10049219 |
| Product codes | HHF |
| Device names | HHF - Remover, Intrauterine Device, Contraceptive, Hook-Type |
| Device class | Class I |
| Classification regulations (21 CFR) | 884.4530 |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | HNM Medical dba HNM TOTAL RECON |
| Establishment registrations | 3009513193 |
| FEI numbers | 3009513193 |
| Establishment operations | Complaint File Establishment, Repackager/Relabeler |
| 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