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Sign in to claim this brandInternational Medical Solutions, Inc.
US
Last updated May 30, 2026
What International Medical Solutions, Inc. makes
International Medical Solutions, Inc. develops radiological Picture Archiving and Communication Systems (PACS) software designed for cloud-based storage and retrieval of medical imaging data. Their solutions facilitate the digital management of radiographic, CT, MRI, and other imaging modalities within healthcare settings.
The company’s portfolio is classified under FDA’s Class II regulatory category and is listed via 510(k) premarket notifications and the FDA’s Unique Device Identifier (UDI) system. These products are intended for use 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 International Medical Solutions, Inc. manufacture?
International Medical Solutions, Inc. specializes in developing radiological Picture Archiving and Communication Systems (PACS) software. These systems are designed for cloud-based storage and retrieval of medical imaging data, including radiographic, CT, MRI, and other imaging modalities. The focus is on enabling healthcare providers to manage digital imaging efficiently within their workflows.
Where is International Medical Solutions, Inc. based?
The company is based in the United States. This geographic location influences its regulatory compliance, particularly with the FDA, as its devices are intended for use within the U.S. market.
Which regulatory registries or databases list devices from International Medical Solutions, Inc.?
Devices from International Medical Solutions, Inc. are listed in the FDA’s 510(k) premarket notification database and the FDA’s Unique Device Identifier (UDI) system. These registries ensure traceability and compliance with U.S. regulatory requirements for Class II devices.
How are the devices produced by International Medical Solutions, Inc. classified by regulatory authorities?
The company’s devices fall under the FDA’s Class II regulatory classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as PACS software that manages critical medical imaging data.
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
- 203073770
Catalogue (4)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BiPro Bicarb Mixing/Distribution System | SDS-CB200 | FDA UDI | Class II | Active |
| CloudVue | 0601 | FDA UDI | Class II | Active |
| Bipro Model Sds-Cb200 | K033118 | FDA 510(k) | Class II | Active |
| CloudVue | K203058 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- International Medical Solutions Inc. Mississauga Ontario · CA FEI 3012391689