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Sign in to claim this brandMEDHAB, LLC
US
Last updated May 24, 2026
What MEDHAB, LLC makes
MedHab, LLC produces pressure-monitoring insoles and sensors designed to detect movement or vibration in beds and chairs. These devices are primarily used to monitor occupant activity, such as pressure distribution and mobility, often in clinical or home care settings. The STEPRITE line includes insoles for foot pressure analysis, while MyNotifi Rx focuses on bed/chair occupant movement detection for patient monitoring purposes.
The company’s products are classified under FDA regulations as either Class I or Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for use in the United States, adhering to applicable regulatory standards for medical devices. No additional international registries or classifications are specified.
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 MedHab, LLC manufacture?
MedHab, LLC specializes in pressure-monitoring devices, including pressure-monitoring insoles (like the STEPRITE line) and sensors that detect movement or vibration in beds and chairs (such as MyNotifi Rx). These devices are designed to analyze pressure distribution and occupant mobility, primarily for clinical or home care monitoring.
Where is MedHab, LLC based, and where are its devices intended for use?
MedHab, LLC is based in the United States. The company’s devices are intended for use within the U.S., where they must comply with applicable FDA regulations. No international regulatory registries or markets are specified for these products.
Which regulatory registries list MedHab, LLC’s devices?
MedHab, LLC’s devices 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. under FDA regulations.
How are MedHab, LLC’s devices classified under FDA regulations?
MedHab, LLC’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve moderate risk and may require special controls to ensure safety and effectiveness. Classification depends on the device’s intended use and potential risk.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 107660874
Catalogue (18)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| RPM2 Rx | 7 Size (00) | FDA UDI | Class II | Unknown |
| Steprite | 7 Size (1) | FDA UDI | Class II | Active |
| RPM2 Rx | 7 Size (2-3) | FDA UDI | Class II | Unknown |
| RPM2 Rx | 7 Size (12) | FDA UDI | Class II | Unknown |
| Steprite | 7 Size (0) | FDA UDI | Class II | Active |
| RPM2 Rx | 7 Size (4) | FDA UDI | Class II | Unknown |
| Steprite | 7 Size (3) | FDA UDI | Class II | Active |
| RPM2 Rx | 7 Size (0) | FDA UDI | Class II | Unknown |
| MyNotifi Rx | Version 2 | FDA UDI | Class I | Active |
| Steprite | 7 Size (2) | FDA UDI | Class II | Active |
| MyNotifi Rx | Version 2 | FDA UDI | Class I | Active |
| RMP2 Rx | 7 Size (1) | FDA UDI | Class II | Unknown |
| Steprite | 7 Size (00) | FDA UDI | Class II | Active |
| RPM2 Rx | 7 Size (2) | FDA UDI | Class II | Unknown |
| Steprite | 7 Size (4) | FDA UDI | Class II | Active |
| RPM2 Rx | 7 Size (01) | FDA UDI | Class II | Unknown |
| RPM2 Rx | 7 Size (3) | FDA UDI | Class II | Unknown |
| MyNotifi Rx | Version 2 | FDA UDI | Class I | Active |
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