FDA device listing
AEX Generator Refurbished
FDA device listing 2029062654 · Medtronic, Inc.
Key facts
| Proprietary names | AEX Generator Refurbished |
|---|---|
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| Premarket submissions | K143175 |
| Product codes | GEI |
| Device names | GEI - Electrosurgical, Cutting & Coagulation & Accessories |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4400 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Medtronic Engineering and Innovation Center (MEIC), MEDTRONIC NAVIGATION, INC., MEDTRONIC POWERED SURGICAL SOLUTIONS, MEDTRONIC SOFAMOR DANEK USA, INC. |
| Establishment registrations | 1625507, 1723170, 3003120897, 3018094310 |
| FEI numbers | 1625507, 1000517638, 3003120897, 3018094310 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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