FDA device listing
Root Apex Locator; C-ROOT I
FDA device listing 1832530608 · Foshan COXO Medical Instrument Co., Ltd.
Key facts
| Proprietary names | Root Apex Locator; C-ROOT I |
|---|---|
| Owner/operator | Foshan COXO Medical Instrument Co., Ltd. |
| Owner/operator number | 10075245 |
| Premarket submissions | K212178 |
| Product codes | LQY |
| Device names | LQY - Locator, Root Apex |
| Device class | Unclassified |
| Classification regulations (21 CFR) | ORCA1.LQY |
| Review panels | Dental |
| Registered establishments | FOSHAN COXO MEDICAL INSTRUMENT CO., LTD. |
| Establishment registrations | 3014953747 |
| FEI numbers | 3014953747 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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