FDA device listing
DENTAL MIRROR, DENTAL MOUTH MIRROR,MirrorSoft No.5 Double Mirror,MirrorSoft No.5 Mirror,MirrorSoft TearDrop…
FDA device listing 1880191068 · Unisource Shanghai Ltd.
Key facts
| Proprietary names | DENTAL MIRROR, DENTAL MOUTH MIRROR,MirrorSoft No.5 Double Mirror,MirrorSoft No.5 Mirror,MirrorSoft TearDrop Mirror,MirroSoft No.4 Mirror |
|---|---|
| Owner/operator | Unisource Shanghai Ltd. |
| Owner/operator number | 10027023 |
| Product codes | EAX |
| Device names | EAX - Mirror, Mouth |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4565 |
| Review panels | Dental |
| Registered establishments | UNISOURCE SHANGHAI LTD. |
| Establishment registrations | 3007165189 |
| FEI numbers | 3007165189 |
| 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