FDA device listing
Bipolar Cautery Cord, da Vinci SP,Cadiere Forceps, da Vinci SP,Camera Sheath, da Vinci SP,Cannula, Circular, 25 mm x 100…
FDA device listing 1917961332 · Intuitive Surgical, Inc.
Key facts
| Proprietary names | Bipolar Cautery Cord, da Vinci SP,Cadiere Forceps, da Vinci SP,Camera Sheath, da Vinci SP,Cannula, Circular, 25 mm x 100 mm, da Vinci SP,Cautery Hook Tip, da Vinci SP,Cautery Spatula Tip, da Vinci SP,Cleaning and Sterilization Kit, da Vinci SP,da Vinci SP Surgical System,da Vinci SP Surgical System, Patient Cart,da Vinci SP Surgical System, Surgeon Console,da Vinci SP Surgical System, Vision… |
|---|---|
| Owner/operator | Intuitive Surgical, Inc. |
| Owner/operator number | 9028901 |
| Premarket submissions | K211316 |
| Product codes | NAY |
| Device names | NAY - System, Surgical, Computer Controlled Instrument |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Bio Analitica Argentina S.A., Cyber Robotic Solutions, S.A de C.V., Device Technologies Australia, DSV Solutions LTD., EXPEDITORS, Expeditors International BV, INTUITIVE SURGICAL, INC., Meditec Venezuela C.A. |
| Establishment registrations | 3001675293, 3005369776, 3010157088, 3010885402, 3011063460, 3013868968, 3015612252, 3016832577, 3020331900, 3042940623 |
| FEI numbers | 3001675293, 3005369776, 3010157088, 3010885402, 3011063460, 3013868968, 3015612252, 3016832577, 3020331900, 3042940623 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 10–99 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 10–99 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