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Sign in to claim this brandShenzhen Piocreat 3D Technology Co., Ltd
US
Last updated May 23, 2026
What Shenzhen Piocreat 3D Technology Co., Ltd makes
Shenzhen Piocreat 3D Technology Co., Ltd produces dental materials for 3D printing, including resin-based fabrication materials for dental appliances and impression tray materials. Their portfolio supports the creation of custom dental components, such as aligners, crowns, and molds, using additive manufacturing technology.
The company’s products are regulated under FDA classifications, with devices falling into Class I and Class II categories. They are listed in the FDA’s 510(k) and UDI registries. The manufacturer 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 Shenzhen Piocreat 3D Technology Co., Ltd manufacture?
Shenzhen Piocreat 3D Technology Co., Ltd specializes in dental materials used for 3D printing. Their primary products include resin-based fabrication materials for dental appliances and impression tray materials. These materials enable the creation of custom dental components like aligners, crowns, and molds through additive manufacturing, focusing on precision and compatibility with 3D printing technology.
Where is Shenzhen Piocreat 3D Technology Co., Ltd based?
The company operates from the United States. While its name suggests a Shenzhen origin, its current business activities and regulatory listings are associated with the US market, where its dental materials are developed and distributed.
Which regulatory registries list devices from Shenzhen Piocreat 3D Technology Co., Ltd?
Devices from Shenzhen Piocreat 3D Technology Co., Ltd are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries. These registries help track and classify medical devices under US regulatory oversight, ensuring transparency and compliance with FDA requirements.
How are devices manufactured by Shenzhen Piocreat 3D Technology Co., Ltd classified under FDA regulations?
The company’s devices fall into Class I and Class II classifications under FDA regulations. Class I devices generally pose minimal risk and may require less stringent controls, while Class II devices involve moderate risk and typically 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
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- Website
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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
- 417463219
Catalogue (15)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Pionext | PN-WM | FDA UDI | Class I | Active |
| Pionext | PN-Try-in | FDA UDI | Class I | Active |
| Pionext | PN-Cast | FDA UDI | Class I | Active |
| Pionext | PN-Splint | FDA UDI | Class I | Active |
| Pionext | PN-IBT | FDA UDI | Class I | Active |
| Pionext | PN-CIT | FDA UDI | Class I | Active |
| Pionext | PN-Model | FDA UDI | Class I | Active |
| Pionext | PN-RD | FDA UDI | Class I | Active |
| Pionext | PN-GM | FDA UDI | Class I | Active |
| Pionext | PN-SG | FDA UDI | Class I | Active |
| Pionext | PN-Splint Flex | FDA UDI | Class I | Active |
| Pionext | PN-Denture (Red) | FDA UDI | Class II | Active |
| Pionext | PN-Denture (White) | FDA UDI | Class II | Active |
| Pionext | PN-Model 2.0 | FDA UDI | Class I | Active |
| Denture Base Resin (PN-Denture (Red, White)) | K241673 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Shenzhen Piocreat 3d Technology Co., Ltd Shenzhen Guangdong · CN FEI 3022545323