FDA device listing
95 mm Stylet
FDA device listing 1359108115 · STRYKER CORP.
Key facts
| Proprietary names | 95 mm Stylet |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Product codes | GAH |
| Device names | GAH - Stylet, Surgical, General & Plastic Surgery |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | NICO CORPORATION, STRYKER GmbH, Stryker Instruments |
| Establishment registrations | 8031020, 3007456622, 3015967359 |
| FEI numbers | 3002807830, 3007456622, 3015967359 |
| 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