FDA device listing
MATERIAL, IMPRESSION TRAY, RESIN
FDA device listing 1533285086 · Tianjin Medicines & Health Products Imp. & Exp. Corp.
Key facts
| Proprietary names | MATERIAL, IMPRESSION TRAY, RESIN |
|---|---|
| Owner/operator | Tianjin Medicines & Health Products Imp. & Exp. Corp. |
| Owner/operator number | 10035880 |
| Product codes | EBH |
| Device names | EBH - Material, Impression Tray, Resin |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.3670 |
| Review panels | Dental |
| Registered establishments | TIANJIN MEDICINES & HEALTH PRODUCTS IMP. & EXP. CORP. |
| Establishment registrations | 1000179416 |
| FEI numbers | 3002468384 |
| Establishment operations | Foreign Exporter |
| 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