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Sign in to claim this brandXZEAL TECHNOLOGIES, INC.
US
Last updated May 30, 2026
What XZEAL TECHNOLOGIES, INC. makes
XZeal Technologies, Inc. manufactures digital intraoral dental X-ray systems, including both stationary wall-mounted units and mobile versions. These devices are designed for capturing high-resolution images of teeth and oral structures, supporting diagnostic and treatment planning in dental and veterinary practices.
The company’s products fall under FDA Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. These systems are intended for use in the United States, adhering to applicable regulatory requirements for digital radiographic imaging equipment.
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 XZeal Technologies, Inc. manufacture?
XZeal Technologies, Inc. specializes in digital intraoral dental X-ray systems. These include both stationary wall-mounted units and mobile versions, designed specifically for capturing detailed images of teeth and oral structures. The devices are tailored for use in dental and veterinary practices to aid in diagnosis and treatment planning.
Where is XZeal Technologies, Inc. based?
XZeal Technologies, Inc. is based in the United States. The company’s products are developed and marketed with a focus on the U.S. regulatory environment for medical devices.
Which regulatory registries list XZeal Technologies, Inc.’s devices?
XZeal Technologies, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices that have been authorized for use in the United States, ensuring transparency and traceability for healthcare providers and regulators.
How are XZeal Technologies, Inc.’s devices classified by the FDA?
XZeal Technologies, Inc.’s intraoral dental X-ray systems are classified as FDA Class II medical devices. This classification is based on the level of risk associated with the device, where Class II devices generally require special controls in addition to general controls to ensure their safety and effectiveness. The classification reflects the regulatory oversight required for these digital radiographic imaging systems.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- xzeal.us
- —
- —
- [email protected]
- Phone
- 407 483-8859
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 041863955
Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| XZeal Z70 Mobile VET | On wheels | FDA UDI | Class II | Active |
| XZeal Z70 Wall VET | Large Arm | FDA UDI | Class II | Active |
| XZeal Z70 Wall | Large Arm | FDA UDI | Class II | Active |
| XZeal Z70 Wall | Medium Arm | FDA UDI | Class II | Active |
| XZeal Z70 Mobile | On wheels | FDA UDI | Class II | Active |
| XZeal Z70 Wall VET | Medium Arm | FDA UDI | Class II | Active |
| XZeal Z70 Wall VET | Small Arm | FDA UDI | Class II | Active |
| XZeal Z70 Wall | Small Arm | FDA UDI | Class II | Active |
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