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US
Last updated May 24, 2026
What PATTERSON TECHNOLOGY CENTER makes
The company develops and maintains Picture Archiving and Communication Systems (PACS) software designed for radiological imaging. These solutions facilitate the storage, retrieval, and distribution of medical images and associated data within healthcare settings, supporting diagnostic workflows and interoperability between imaging devices and clinical systems.
The portfolio consists of Class II medical devices, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The company’s products are regulated under U.S. FDA guidelines 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 Patterson Technology Center manufacture?
Patterson Technology Center specializes in developing Picture Archiving and Communication Systems (PACS) software for radiological imaging. These systems are designed to store, retrieve, and distribute medical images and related data, enabling seamless workflows in healthcare environments. The company’s focus is exclusively on software-based solutions in this category.
Where is Patterson Technology Center based, and how does this affect its regulatory oversight?
Patterson Technology Center is based in the United States. Since its devices are regulated under U.S. FDA guidelines, they must comply with the agency’s requirements for medical devices. The company’s location ensures alignment with FDA-specific regulations, including mandatory listing in the FDA’s Unique Device Identifier (UDI) database for its Class II devices.
Which regulatory registries or databases list Patterson Technology Center’s devices?
Patterson Technology Center’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is a central repository for identifying medical devices in the U.S., ensuring traceability and compliance with FDA requirements. Listing in the UDI database is mandatory for Class II devices, which includes Patterson Technology Center’s entire portfolio.
How are Patterson Technology Center’s devices classified under FDA regulations?
Patterson Technology Center’s devices are classified as Class II under FDA regulations. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness. The company’s PACS software falls under this category due to its role in managing critical radiological imaging data, necessitating validation of performance and compliance with FDA guidelines.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- pattersoncompanies.com
- —
- —
- [email protected]
- Phone
- (818) 435-1846
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 062232311
Catalogue (42)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Eaglesoft | 19.10 | FDA UDI | Class II | Active |
| Eaglesoft | 21.20 | FDA UDI | Class II | Active |
| Eaglesoft | 18.10 | FDA UDI | Class II | Active |
| Eaglesoft | 19.00 | FDA UDI | Class II | Active |
| Eaglesoft | 21.10 | FDA UDI | Class II | Active |
| Eaglesoft | 20.10 | FDA UDI | Class II | Active |
| Fuse | 1.09 | FDA UDI | Class II | Unknown |
| Fuse | 1.00 | FDA UDI | Class II | Active |
| Eaglesoft | 21.00 | FDA UDI | Class II | Active |
| Eaglesoft | 21.20 | FDA UDI | Class II | Active |
| Eaglesoft | 21.10 | FDA UDI | Class II | Active |
| Fuse | 1.03 | FDA UDI | Class II | Active |
| Fuse | 1.08 | FDA UDI | Class II | Active |
| Eaglesoft | 18.10 | FDA UDI | Class II | Active |
| Eaglesoft | 21.10 | FDA UDI | Class II | Active |
| Eaglesoft | 19.10 | FDA UDI | Class II | Active |
| Eaglesoft | 21.00 | FDA UDI | Class II | Active |
| Fuse | 1.06 | FDA UDI | Class II | Active |
| Eaglesoft | 21.20 | FDA UDI | Class II | Active |
| Eaglesoft | 21.20 | FDA UDI | Class II | Active |
| Fuse | 1.01 | FDA UDI | Class II | Active |
| Fuse | 1.02 | FDA UDI | Class II | Active |
| Eaglesoft | 21.10 | FDA UDI | Class II | Active |
| Fuse | 1.04 | FDA UDI | Class II | Active |
| Eaglesoft | 18.10 | FDA UDI | Class II | Active |
| Eaglesoft | 18.10 | FDA UDI | Class II | Active |
| Eaglesoft | 21.20 | FDA UDI | Class II | Active |
| Fuse | 1.07 | FDA UDI | Class II | Active |
| Eaglesoft | 21.20 | FDA UDI | Class II | Active |
| Eaglesoft | 21.00 | FDA UDI | Class II | Active |
| Eaglesoft | 18.10 | FDA UDI | Class II | Active |
| Eaglesoft | 19.10 | FDA UDI | Class II | Active |
| Eaglesoft | 21.10 | FDA UDI | Class II | Active |
| Eaglesoft | 18.10 | FDA UDI | Class II | Active |
| Eaglesoft | 21.00 | FDA UDI | Class II | Active |
| Eaglesoft | 20.00 | FDA UDI | Class II | Active |
| Eaglesoft | 18.10 | FDA UDI | Class II | Active |
| Eaglesoft | 21.20 | FDA UDI | Class II | Active |
| Eaglesoft | 23 | FDA UDI | Class II | Active |
| Fuse | 1.05 | FDA UDI | Class II | Active |
| Eaglesoft | 21.10 | FDA UDI | Class II | Active |
| Eaglesoft | 21.00 | FDA UDI | Class II | Active |
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