FDA device listing
Dual Flat Panel (FP) Yoke Suspension,Flexis Boom System,HipCheck Table Mount,Light Duty Suspension,Medium Duty Dual…
FDA device listing 1711863728 · STRYKER CORP.
Key facts
| Proprietary names | Dual Flat Panel (FP) Yoke Suspension,Flexis Boom System,HipCheck Table Mount,Light Duty Suspension,Medium Duty Dual Yoke,Medium Duty Suspension,Monitor Ceiling Suspension (MCS) Boom System,Monitor Mount,Navigation System Suspension,Single Universal Flat Panel Suspension,S-Series Equipment Management System,TELETOM Equipment Management System |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Product codes | FQO |
| Device names | FQO - Table, Operating-Room, Ac-Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4960 |
| Review panels | General & Plastic Surgery |
| Registered establishments | STRYKER Communications, Inc., STRYKER ENDOSCOPY |
| Establishment registrations | 2031963, 2936485 |
| FEI numbers | 2936485, 3002975342 |
| Establishment operations | Complaint File Establishment, Manufacturer, 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