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Sign in to claim this brandQUALITY MEDICAL SUPPLY, INC.
US
Last updated May 27, 2026
What QUALITY MEDICAL SUPPLY, INC. makes
Quality Medical Supply, Inc. manufactures colonic lavage devices, including non-surgical lavage kits and standalone lavage units designed for bowel preparation. Their product line includes both disposable and reusable systems, tailored for clinical and home use.
The company’s devices are classified under FDA categories Class I and Class II, with submissions recorded in the FDA’s 510(k) and UDI registries. These products are listed under U.S. regulatory frameworks and are based in 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 Quality Medical Supply, Inc. manufacture?
Quality Medical Supply, Inc. specializes in colonic lavage devices, which are used for bowel preparation. Their product line includes non-surgical colonic lavage kits and standalone colonic lavage units. These devices are designed for both clinical and home use, with variations tailored for disposable or reusable systems.
Where is Quality Medical Supply, Inc. based?
Quality Medical Supply, Inc. is headquartered in the United States. This location aligns with the regulatory frameworks under which their devices are listed, including the FDA’s 510(k) and UDI systems.
Which regulatory registries list devices manufactured by Quality Medical Supply, Inc.?
Devices from Quality Medical Supply, Inc. are recorded in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identifier (UDI) system. These registries track submissions for Class I and Class II devices, ensuring compliance with U.S. medical device regulations.
How are the devices made by Quality Medical Supply, Inc. classified under FDA regulations?
The devices produced by Quality Medical Supply, Inc. fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The specific classification depends on the device’s design and intended use.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- qmsaz.com
- —
- —
- [email protected]
- Phone
- 6236404646
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 969138283
Catalogue (18)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Qms - 42cfhy | 01 | FDA UDI | Class I | Active |
| Qms - 48sbhy | 01 | FDA UDI | Class I | Active |
| Qms - 42cfsp | 01 | FDA UDI | Class I | Active |
| Qms - 42cfop | 01 | FDA UDI | Class I | Active |
| Qms - 48cfsp | 01 | FDA UDI | Class I | Active |
| Qms - 42sbst | 01 | FDA UDI | Class I | Active |
| Qms - 48sbsp | 01 | FDA UDI | Class I | Active |
| Qms - 42sbhy | 01 | FDA UDI | Class I | Active |
| Qms - 42cfst | 01 | FDA UDI | Class I | Active |
| Qms - 48cfop | 01 | FDA UDI | Class I | Active |
| Qms - 48sbst | 01 | FDA UDI | Class I | Active |
| Qms - Aqua Cleanse | 01 | FDA UDI | Class II | Active |
| Qms - 48cfst | 01 | FDA UDI | Class I | Active |
| Qms - 48sbop | 01 | FDA UDI | Class I | Active |
| Qms - 42sbsp | 01 | FDA UDI | Class I | Active |
| Qms - 48cfhy | 01 | FDA UDI | Class I | Active |
| Qms - 42sbop | 01 | FDA UDI | Class I | Active |
| Aqua Cleanse | K150381 | FDA 510(k) | Class II | Active |
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