FDA device listing
Colonic Irrigation Devices,LIBBE Colon Hydrotherapy-Lower Bowel Evacuation System,LIBBE Colon Hydrotherapy System,LIBBE…
FDA device listing 1293381772 · TILLER MIND BODY, INC.
Key facts
| Proprietary names | Colonic Irrigation Devices,LIBBE Colon Hydrotherapy-Lower Bowel Evacuation System,LIBBE Colon Hydrotherapy System,LIBBE Colonic Irrigation System |
|---|---|
| Owner/operator | TILLER MIND BODY, INC. |
| Owner/operator number | 9011577 |
| Premarket submissions | K941279 |
| Product codes | KPL |
| Device names | KPL - Colonic Irrigation System |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.5220 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | TILLER MIND BODY, INC. |
| Establishment registrations | 1648139 |
| FEI numbers | 1000516428 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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