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Sign in to claim this brandEDDA Technology, Inc.
US
Last updated September 17, 2026
What EDDA Technology, Inc. makes
EDDA Technology, Inc. develops software applications for processing and analyzing DICOM medical images, including tools for quality assurance and diagnostic support in radiology. Their portfolio includes specialized software packages for liver and chest imaging, designed to enhance multimodality analysis and improve workflow efficiency in clinical settings.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. EDDA Technology, 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.
Information
- Country
- US
- Address
- 5 Independence Way, Princeton, NJ, 08540
- 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
- 3004857110
- DUNS Number
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Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Edda Technology | IQQA-Liver Multimodality | FDA UDI | Class II | Active |
| Edda Technology | IQQA-Chest | FDA UDI | Class II | Active |
| Edda Technology | IQQA-Liver | FDA UDI | Class II | Active |
| Edda Technology | IQQA-Guide | FDA UDI | Class II | Active |
| Edda Technology | IQQA-BodyImaging | FDA UDI | Class II | Active |
| Biolumin. Screening For Bact. By Atp A. | K803077 | FDA 510(k) | N/A | Active |
| Iqqa-Liver Software | K061696 | FDA 510(k) | Class II | Active |
| Iqqa-Bodyimaging Software | K141745 | FDA 510(k) | Class II | Active |
| Iqqa-Chest Software Package | K042408 | FDA 510(k) | Class II | Active |
| Iqqa-Liver Multimodality Software | K131498 | FDA 510(k) | Class II | Active |
| IQQA Guide | K151414 | FDA 510(k) | Class II | Active |
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