FDA device listing
100MM DRAIN CANNULA,10MM DRAIN CANNULA,1.3MM X 35.6CM NITINOL GUIDE WIRE,1.9MM OBTURATOR,1.9MM SPEEDLOCK PENCIL TIP…
FDA device listing 1962748967 · STRYKER CORP.
Key facts
| Proprietary names | 100MM DRAIN CANNULA,10MM DRAIN CANNULA,1.3MM X 35.6CM NITINOL GUIDE WIRE,1.9MM OBTURATOR,1.9MM SPEEDLOCK PENCIL TIP OBTURATOR,1.9MM TROCAR,2-0 Knot Pusher/Suture Cutter,2.1MM BLUNT NOSE DOWN ASSY,2.1MM BLUNT NOSE LEFT ASSY,2.1MM BLUNT NOSE RIGHT ASSY,2.1MM BLUNT NOSE STRAIGHT ASSY,2.1MM BLUNT NOSE UP ASSY,2.3MM AUTOCLAVABLE BLUNT TIP OBTURATOR WITH SPEED-LOCK,2.3MM AUTOCLAVABLE PENCIL TIP… |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Product codes | NBH |
| Device names | NBH - Accessories, Arthroscopic |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.1100 |
| Review panels | Orthopedic |
| Registered establishments | HOWMEDICA OSTEONICS CORP, STRYKER EMEA Supply Chain Services, STRYKER ENDOSCOPY, STRYKER GmbH |
| Establishment registrations | 2249697, 2936485, 8031020, 3008837339 |
| FEI numbers | 2936485, 3002807830, 3003070421, 3008837339 |
| Establishment operations | Complaint File Establishment, Manufacturer, Foreign Exporter, 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