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Sign in to claim this brandE-Pros Co., Ltd.
US
Last updated May 24, 2026
What E-Pros Co., Ltd. makes
E-Pros Co., Ltd. manufactures single-use dental implant abutment analogs designed for intraoral scanning, including components like the Truss Lab Analog and Truss Screw. Their products also include scanning jigs, such as the Truss Scanjig, which assist in precise digital impressions for dental restorations.
These devices are classified as Class I and Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from 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 E-Pros Co., Ltd. manufacture?
E-Pros Co., Ltd. specializes in dental implant-related devices, specifically single-use dental implant abutment analogs and intraoral scanning tools. Their products include analogs like the Truss Lab Analog, scanning jigs (e.g., Truss Scanjig), and screws (e.g., Truss Screw). These devices are primarily used in digital dental workflows to create precise impressions for restorations.
Where is E-Pros Co., Ltd. based?
E-Pros Co., Ltd. is headquartered in the United States. The company’s location is relevant for regulatory compliance, manufacturing oversight, and customer support in North America.
Which regulatory registries or databases list E-Pros Co., Ltd.’s devices?
E-Pros Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, insurers, and regulatory authorities tracking specific medical devices.
How are E-Pros Co., Ltd.’s devices classified under FDA regulations?
E-Pros Co., Ltd.’s devices fall under Class I and Class II classifications under FDA regulations. Class I devices generally pose minimal risk and often require less regulatory scrutiny, while Class II devices involve moderate risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential health impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- [email protected]
- Phone
- +820535228778
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 963196443
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Truss Lab Analog | TR-A | FDA UDI | Class I | Active |
| Truss Scanjig | TN-2003 | FDA UDI | Class I | Active |
| Truss Scanjig | TR-2003 | FDA UDI | Class I | Active |
| Truss Scanjig | UFO | FDA UDI | Class I | Active |
| Truss Lab Analog | TN-A | FDA UDI | Class I | Active |
| Truss Lab Analog | TS-A | FDA UDI | Class II | Active |
| Truss Lab Analog | TM-A | FDA UDI | Class I | Active |
| Truss Screw | SCREW | FDA UDI | Class I | Active |
| Truss Scanjig | TM-2003 | FDA UDI | Class I | Active |
| Truss Scanjig | TS-2003 | FDA UDI | Class I | Active |
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