FDA device listing
kage Cushion, denture, over the counter
FDA device listing 1408028469 · one day dental partner
Key facts
| Proprietary names | kage Cushion, denture, over the counter |
|---|---|
| Owner/operator | one day dental partner |
| Owner/operator number | 10095050 |
| Product codes | EHS |
| Device names | EHS - Cushion, Denture, Over The Counter |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.3540 |
| Review panels | Dental |
| Registered establishments | ONE DAY DENTAL PARTNER |
| Establishment registrations | 3043303267 |
| FEI numbers | 3043303267 |
| Establishment operations | Foreign Exporter, 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