FDA device listing
Anyplus II Implant Tray,Anyplus II Instrument Tray (1/2),New Anyplus II Prebent Rod Caddy,PYXIS 3D Titanium Cervical…
FDA device listing 1792341854 · GS Solutions, Inc.
Key facts
| Proprietary names | Anyplus II Implant Tray,Anyplus II Instrument Tray (1/2),New Anyplus II Prebent Rod Caddy,PYXIS 3D Titanium Cervical Cage Instruments Tray,Tray,Universal Removal Set Tray |
|---|---|
| Owner/operator | GS Solutions, Inc. |
| Owner/operator number | 9080979 |
| Product codes | FSM |
| Device names | FSM - Tray, Surgical, Instrument |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | GS MEDICAL CO., LTD. |
| Establishment registrations | 3005596514 |
| FEI numbers | 3005596514 |
| Establishment operations | Manufacturer |
| 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