FDA device listing
Rite Aid Electric Nasal Irrigator
FDA device listing 1654376035 · ToLife Technologies Pty Ltd
Key facts
| Proprietary names | Rite Aid Electric Nasal Irrigator |
|---|---|
| Owner/operator | ToLife Technologies Pty Ltd |
| Owner/operator number | 10048898 |
| Product codes | KMA |
| Device names | KMA - Irrigator, Powered Nasal |
| Device class | Class I |
| Classification regulations (21 CFR) | 874.5550 |
| Review panels | Ear, Nose, & Throat |
| Registered establishments | TOLIFE TECHNOLOGIES PTY LTD |
| Establishment registrations | 3011553249 |
| FEI numbers | 3011553249 |
| Establishment operations | 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