FDA device listing
Belmont
FDA device listing 1935729794 · TAKARA BELMONT CORPORATION
Key facts
| Proprietary names | Belmont |
|---|---|
| Owner/operator | TAKARA BELMONT CORPORATION |
| Owner/operator number | 8031613 |
| Product codes | EAZ |
| Device names | EAZ - Light, Operating, Dental |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4630 |
| Review panels | Dental |
| Registered establishments | Belmont Manufacturing Co., Ltd., BELMONT TECHNO KYOTO CORPORATION, TAKARA BELMONT CORPORATION, TAKARA BELMONT CORPORATION, OSAKA FACTORY |
| Establishment registrations | 9611445, 3009774128, 3014766731, 3029972406 |
| FEI numbers | 3002808310, 3009774128, 3014766731, 3029972406 |
| Establishment operations | Complaint File Establishment, Manufacturer, Specification Developer, Contract 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