FDA device listing
Reprocessed Monopolar and Bipolar Electrosurgical Cutting and Coagulation Devices,SURETEK REPROCESSED ELE
FDA device listing 1703342287 · SURETEK MEDICAL
Key facts
| Proprietary names | Reprocessed Monopolar and Bipolar Electrosurgical Cutting and Coagulation Devices,SURETEK REPROCESSED ELE |
|---|---|
| Owner/operator | SURETEK MEDICAL |
| Owner/operator number | 9082027 |
| Premarket submissions | K052690 |
| Product codes | NUJ |
| Device names | NUJ - Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4400 |
| Review panels | General & Plastic Surgery |
| Registered establishments | SURETEK MEDICAL |
| Establishment registrations | 3005575604 |
| FEI numbers | 3005575604 |
| Establishment operations | Reprocessor of Single Use Devices |
| 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