FDA device listing
10-100 Nasal Pack - 4.5cm,10101C Nasal Pack Classic, with drawstring 4.5cm,10-101 Nasal Slimpack - 4.5cm,10-105 Nasal…
FDA device listing 1323287736 · SWANN MORTON, LTD.
Key facts
| Proprietary names | 10-100 Nasal Pack - 4.5cm,10101C Nasal Pack Classic, with drawstring 4.5cm,10-101 Nasal Slimpack - 4.5cm,10-105 Nasal Pack 6.0cm,10-105T Nasal Pack with Tube - 6.0cm,10-106 Nasal Slimpack 6cm,10-110 Nasal Pack - 8.0cm,10-110T Nasal Pack with Tube - 8.0cm,10111C Nasal Pack, with drawstring - 8.0cm,10111L Nasal Pack, with drawstring, multi-layered - 8.0cm,10-111 Nasal slimpack - 8.0 cm,10-111T Nasal… |
|---|---|
| Owner/operator | SWANN MORTON, LTD. |
| Owner/operator number | 9003320 |
| 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 | Swann-Morton(Services) Limited |
| Establishment registrations | 3008812251 |
| FEI numbers | 3002808293 |
| Establishment operations | Contract Sterilizer |
| 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