FDA device listing
Valleylab™ Laparoscopic Curved Spatula Electrode, Hollow, 28 cm, E2781-28,Valleylab™ Laparoscopic Curved Spatula…
FDA device listing 1237547278 · Medtronic, Inc.
Key facts
| Proprietary names | Valleylab™ Laparoscopic Curved Spatula Electrode, Hollow, 28 cm, E2781-28,Valleylab™ Laparoscopic Curved Spatula Electrode, Retractable, Aspiration Holes, 28 cm, E2781R-28ASP,Valleylab™ Laparoscopic Cylindrical Electrode, Hollow, 28 cm, E2786-28,Valleylab™ Laparoscopic Flat L-Hook Electrode, Hollow, 28 cm, E2784-28,Valleylab™ Laparoscopic Flat L-Hook Electrode, Retractable, Aspiration Holes, 28… |
|---|---|
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| Premarket submissions | K964175 |
| 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) |
| Establishment registrations | 3018094310 |
| FEI numbers | 3018094310 |
| Establishment operations | Complaint File Establishment |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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