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Sign in to claim this brandProvidus Holdings, Inc.
US
Last updated May 24, 2026
What Providus Holdings, Inc. makes
The company manufactures phantoms and test objects for medical imaging and radiation therapy, including CT, MRI, and diagnostic X-ray phantoms. These products are designed for quality assurance, calibration, and performance testing in clinical and research settings. Examples include anthropomorphic and non-anthropomorphic phantoms for multi-modality imaging and therapeutic radiation, as well as specialized phantoms like the liver phantom and liquid-filled calibration objects.
The portfolio consists of Class I medical devices, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates under US regulatory oversight, adhering to applicable standards for imaging and radiation phantoms.
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 Providus Holdings, Inc. manufacture?
Providus Holdings, Inc. specializes in phantoms and test objects used for quality assurance, calibration, and performance testing in medical imaging and radiation therapy. Their devices include CT phantoms, MRI phantoms, diagnostic X-ray phantoms, and specialized phantoms like anthropomorphic (human-shaped) models for multi-modality imaging (e.g., CT, MRI, and radiation therapy) as well as non-anthropomorphic test objects. Examples include the Magphan®, Catphan®, and LiquiPhil™, which are designed to simulate human tissue properties for accurate equipment validation.
Where is Providus Holdings, Inc. based, and under which regulatory framework do their devices operate?
Providus Holdings, Inc. is based in the United States. Their devices fall under U.S. regulatory oversight, specifically as Class I medical devices, which are generally considered to pose the lowest risk. Since these devices are classified as Class I, they are subject to the FDA’s listing requirements, including registration in the FDA’s Unique Device Identifier (UDI) database (fda_udi). This classification reflects their intended use for quality assurance and calibration purposes, where minimal risk to patients is involved.
Which regulatory registries or databases list Providus Holdings, Inc.’s devices?
Providus Holdings, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database (fda_udi). This registry is maintained to track and identify medical devices authorized for commercial distribution in the U.S. The inclusion of their phantoms and test objects in this database aligns with their classification as Class I devices, which require UDI labeling and FDA listing to ensure traceability and compliance with regulatory standards.
How are Providus Holdings, Inc.’s devices classified under U.S. regulations?
Providus Holdings, Inc.’s devices are classified as Class I medical devices under U.S. regulations. This classification is determined by the FDA based on the intended use of the devices—specifically, their role in quality assurance, calibration, and performance testing for medical imaging and radiation therapy equipment. Class I devices are generally considered to have minimal risk to patients and users, which is why they require the least regulatory oversight beyond general controls, including UDI listing and compliance with applicable standards.
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
- 104162493
Catalogue (87)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Catphan® | CTP682 | FDA UDI | Class I | Active |
| Rando® | XA231P | FDA UDI | Class I | Active |
| Catphan® | CTP346 | FDA UDI | Class I | Active |
| Catphan® | CTP700 | FDA UDI | Class I | Active |
| LiquiPhil™ | TLP131 | FDA UDI | Class I | Active |
| LiquiPhil™ | DDP010 | FDA UDI | Class I | Active |
| Catphan® | CTP579-20 | FDA UDI | Class I | Active |
| Catphan® | CTP528 | FDA UDI | Class I | Active |
| Catphan® | CTP508 | FDA UDI | Class I | Active |
| Magphan® | SMR172 | FDA UDI | Class I | Active |
| Rando® | XA241R | FDA UDI | Class I | Active |
| Rando® | XA235R | FDA UDI | Class I | Active |
| Catphan® | CTP606 | FDA UDI | Class I | Active |
| Rando® | XA245L | FDA UDI | Class I | Active |
| Low Contrast MITA Head Phantom | CCT191 | FDA UDI | Class I | Active |
| Magphan® | SMR100 | FDA UDI | Class I | Active |
| ECTphan™ | SMR352 | FDA UDI | Class I | Active |
| ECTphan™ | SMR357 | FDA UDI | Class I | Active |
| Catphan® | CTP579 | FDA UDI | Class I | Active |
| LiquiPhil™ | TLP280 | FDA UDI | Class I | Active |
| LiquiPhil™ | TLP134 | FDA UDI | Class I | Active |
| Catphan® | CTP504 | FDA UDI | Class I | Active |
| LiquiPhil™ | TLP133 | FDA UDI | Class I | Active |
| Catphan® | CTP650 | FDA UDI | Class I | Active |
| ECTphan™ | SMR350 | FDA UDI | Class I | Active |
| Catphan® | CTP343 | FDA UDI | Class I | Active |
| Catphan® | CCT162 | FDA UDI | Class I | Active |
| Catphan® | CTP651-10 | FDA UDI | Class I | Active |
| Rando® | XA235L | FDA UDI | Class I | Active |
| Catphan® | CTP651-20 | FDA UDI | Class I | Active |
| Catphan® | CTP651 | FDA UDI | Class I | Active |
| LiquiPhil™ | TLP227 | FDA UDI | Class I | Active |
| Catphan® | CTP650-15 | FDA UDI | Class I | Active |
| Corgi® | CGI014 | FDA UDI | Class I | Active |
| Catphan® | CTP451 | FDA UDI | Class I | Active |
| Catphan® | CTP754 | FDA UDI | Class I | Active |
| Catphan® | CTP653 | FDA UDI | Class I | Active |
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