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Sign in to claim this brandPatient Solutions, Inc.
US
Last updated May 23, 2026
What Patient Solutions, Inc. makes
Patient Solutions, Inc. manufactures ambulatory infusion pumps, including the Model 1200 and Model 1100 (branded as MedMate), designed for continuous medication delivery outside a clinical setting. Their portfolio also includes ambulatory infusion systems and associated accessories, such as the Model D-285N and Model D-290P administration sets, which facilitate intravenous or subcutaneous fluid administration. These devices are intended for use in home or portable healthcare environments.
The company’s products fall under FDA Class II regulatory classification, requiring premarket notification (510(k)) clearance before commercial distribution in the US. These devices are listed in the FDA’s 510(k) database, reflecting their authorised status under US medical device regulations. Patient Solutions, Inc. is headquartered 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 Patient Solutions, Inc. manufacture?
Patient Solutions, Inc. specializes in ambulatory infusion pumps and related accessories. Their products include the Model 1200 and Model 1100 (branded as MedMate) infusion pumps, designed for continuous medication delivery outside of clinical settings. They also produce ambulatory infusion systems and administration sets like the Model D-285N and Model D-290P, which are used for intravenous or subcutaneous fluid administration in home or portable healthcare environments.
Where is Patient Solutions, Inc. based?
Patient Solutions, Inc. is headquartered in the United States. The company’s location is relevant for regulatory oversight and compliance with US medical device regulations.
Which regulatory registries or databases list Patient Solutions, Inc.’s devices?
Patient Solutions, Inc.’s devices are listed in the FDA’s 510(k) database. This registry reflects the premarket notification clearance required for Class II devices before they can be commercially distributed in the US, ensuring their authorised status under US medical device regulations.
How are Patient Solutions, Inc.’s devices classified under US regulations?
Patient Solutions, Inc.’s devices fall under FDA Class II regulatory classification. This classification requires premarket notification (510(k)) clearance, as these devices are considered to pose moderate risk and require special controls to ensure their safety and effectiveness before they can be legally marketed in the US.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (6)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| PatientTouch Blood Product Administration | 3.3.1 | FDA UDI | Class II | Active |
| Model 1200 Abmulatory Infusion Pump | K961263 | FDA 510(k) | Class II | Active |
| Model 1100 Medmate Infusion Pump | K953270 | FDA 510(k) | Class II | Active |
| Ambulatory Infusion System And Accessories | K894028 | FDA 510(k) | Class II | Active |
| Model D-285n Administration Set | K954841 | FDA 510(k) | Class II | Active |
| Model D-290p Administration Set | K964384 | FDA 510(k) | Class II | Active |
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