FDA device listing
GUEDEL AIRWAY,LARYSEAL LARYNGEAL MASK,LARYSEAL PLUS LARYNGEAL MASK AIRWAY,LARYSEAL PRO LARYNGEAL MASK,Williams Airway
FDA device listing 1071559551 · FLEXICARE MEDICAL LTD.
Key facts
| Proprietary names | GUEDEL AIRWAY,LARYSEAL LARYNGEAL MASK,LARYSEAL PLUS LARYNGEAL MASK AIRWAY,LARYSEAL PRO LARYNGEAL MASK,Williams Airway |
|---|---|
| Owner/operator | FLEXICARE MEDICAL LTD. |
| Owner/operator number | 8021995 |
| Product codes | CAE |
| Device names | CAE - Airway, Oropharyngeal, Anesthesiology |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5110 |
| Review panels | Anesthesiology |
| Registered establishments | FLEXICARE MEDICAL (DONGGUAN) LTD., FLEXICARE MEDICAL LTD. |
| Establishment registrations | 8021995, 3006061749 |
| FEI numbers | 3006061749, 3006363476 |
| Establishment operations | Contract Manufacturer, 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