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Sign in to claim this brandMind Body Naturopathic Inst
US
Last updated May 30, 2026
What Mind Body Naturopathic Inst makes
The company manufactures colonic lavage devices, including sterile nozzles and gravity-flow systems designed for colon hydrotherapy procedures. These products are intended for use in clinical or therapeutic settings to facilitate the cleansing of the colon.
The portfolio consists of Class II medical devices, listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Mind Body Naturopathic Inst manufacture?
Mind Body Naturopathic Inst specializes in colonic lavage devices, which include sterile nozzles and gravity-flow systems. These products are specifically designed for colon hydrotherapy procedures, intended to cleanse the colon in clinical or therapeutic settings. The focus is on devices that assist in medical or wellness-related colon care.
Where is Mind Body Naturopathic Inst based, and how does that affect its devices?
Mind Body Naturopathic Inst is based in the United States. This location means its devices are subject to U.S. regulatory requirements, including classification and listing in the FDA’s Unique Device Identifier (UDI) database. The company’s devices are designed and manufactured in compliance with applicable U.S. regulations for medical devices.
Which regulatory registries or databases list the devices made by Mind Body Naturopathic Inst?
The devices produced by Mind Body Naturopathic Inst are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.
How are the devices manufactured by Mind Body Naturopathic Inst classified under U.S. regulations?
The devices from Mind Body Naturopathic Inst fall under Class II classification in the U.S. regulatory system. This classification applies to devices that generally pose moderate risk and require special controls to ensure their safety and effectiveness, such as colonic lavage systems and nozzles used in colon hydrotherapy.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- colonic.net
- —
- —
- [email protected]
- Phone
- (210)308-8888
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 929869659
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LIBBE Colonic Nozzle | 298-8888 | FDA UDI | Class II | Active |
| LIBBE Colon Hydrotherapy System | 9703 | FDA UDI | Class II | Active |
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