FDA device listing
Cure Foam 3DS,Cure Foam 5DS,Cure Foam 7DS,Nasalvo,NS Cavity Splint,NS Flex Splint,NS Hard Splint,NS soft Splint
FDA device listing 1311491515 · Dmed
Key facts
| Proprietary names | Cure Foam 3DS,Cure Foam 5DS,Cure Foam 7DS,Nasalvo,NS Cavity Splint,NS Flex Splint,NS Hard Splint,NS soft Splint |
|---|---|
| Owner/operator | Dmed |
| Owner/operator number | 10037526 |
| Product codes | LYA |
| Device names | LYA - Splint, Intranasal Septal |
| Device class | Class I |
| Classification regulations (21 CFR) | 874.4780 |
| Review panels | Ear, Nose, & Throat |
| Registered establishments | DMED |
| Establishment registrations | 3009134882 |
| FEI numbers | 3009134882 |
| Establishment operations | 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