FDA device listing
ROD BENDER
FDA device listing 1825925704 · Medtronic, Inc.
Key facts
| Proprietary names | ROD BENDER |
|---|---|
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| Product codes | HXP |
| Device names | HXP - Instrument, Bending Or Contouring |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4540 |
| Review panels | Orthopedic |
| Registered establishments | Medtronic (Changzhou) Medical Devices Technology Co., Ltd, Medtronic Engineering and Innovation Center (MEIC), MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO, MEDTRONIC SOFAMOR DANEK USA, INC., WARSAW ORTHOPEDIC, INC. |
| Establishment registrations | 1030489, 1824199, 2647346, 3003120897, 3005677016, 3018094310 |
| FEI numbers | 1824199, 2647346, 1000477302, 3003120897, 3005677016, 3018094310 |
| Establishment operations | Complaint File Establishment, Manufacturer, Repackager/Relabeler, Specification Developer |
| 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