FDA device listing
Vista Disposable HVE Screens
FDA device listing 2066682416 · INTER-MED, INC.
Key facts
| Proprietary names | Vista Disposable HVE Screens |
|---|---|
| Owner/operator | INTER-MED, INC. |
| Owner/operator number | 9025886 |
| Product codes | DYN |
| Device names | DYN - Mouthpiece, Saliva Ejector |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.6640 |
| Review panels | Dental |
| Registered establishments | INTER-MED, INC., SINO-VISTA DENTAL INSTRUMENTS CO., LTD. |
| Establishment registrations | 2133714, 3006608997 |
| FEI numbers | 3000209941, 3006608997 |
| Establishment operations | Contract Manufacturer, Repackager/Relabeler, Specification Developer |
| 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