FDA device listing
Vista S70 Apical Surgery Tip,Vista S70D Apical Surgery Tip,Vista S90 Apical Surgery Tip,Vista S90D Apical Surgery…
FDA device listing 1019334941 · INTER-MED, INC.
Key facts
| Proprietary names | Vista S70 Apical Surgery Tip,Vista S70D Apical Surgery Tip,Vista S90 Apical Surgery Tip,Vista S90D Apical Surgery Tip,Vista SA Apical Surgery Tip,Vista SAD Apical Surgery Tip,Vista SML Apical Surgery Tip,Vista SMLD Apical Surgery Tip,Vista SMR Apical Surgery Tip,Vista SMRD Apical Surgery Tip,Vista SPL Apical Surgery Tip,Vista SPLD Apical Surgery Tip,Vista SPR Apical Surgery Tip,Vista SPRD Apical… |
|---|---|
| Owner/operator | INTER-MED, INC. |
| Owner/operator number | 9025886 |
| Product codes | EMK |
| Device names | EMK - Curette, Surgical, Dental |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4565 |
| Review panels | Dental |
| Registered establishments | INTER-MED, INC. |
| Establishment registrations | 2133714 |
| FEI numbers | 3000209941 |
| Establishment operations | 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