FDA device listing
Product: OJG - Neurological tray
FDA device listing 1175911265 · Takayama Instrument, Inc.
Key facts
| Proprietary names | Product: OJG - Neurological tray |
|---|---|
| Owner/operator | Takayama Instrument, Inc. |
| Owner/operator number | 10050133 |
| Product codes | OJG |
| Device names | OJG - Neurological Tray |
| Device class | Class I |
| Classification regulations (21 CFR) | 882.4525 |
| Review panels | Neurology |
| Registered establishments | TAKAYAMA INSTRUMENT INC. |
| Establishment registrations | 3010635845 |
| FEI numbers | 3010635845 |
| Establishment operations | Complaint File Establishment, 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