Manufacturer registered with FDA
Shenzhen Piocreat 3D Technology Co., Ltd
Shenzhen, China. Lists 6 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 6
- Brands and models
- 7
- 510(k) clearances
- 12024–2024
- Markets registered in
- 1United States
- Establishments
- 1China
510(k) clearances per year, 2007–2026
Devices listed with FDA
What Shenzhen Piocreat 3D Technology Co., Ltd currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Resin Tooth Shade MaterialEBF · Class 2 | Dental composites | Maker | Denture Base Resin(PN-Denture (Red,White)) | 2024 |
| Resin Temporary Crown and BridgeEBG · Class 2 | Temporary crown & bridge materials | Maker | Denture Base Resin(PN-Denture (Red,White)) | 2024 |
| Resin Impression Tray MaterialEBH · Class 1 | Impression trays | Maker | PioNext Dental Model Resin (Models: PN-IBT, PN-Try-in, PN-Splint, PN-Splint Flex)PioNext Dental Model Resin (Models: PN-Model, PN-Model 2, PN-RD, PN-WM, PN-CIT, PN-SG, PN-Cast, PN-GM) | 2023 |
| Rebasing Repairing Relining Denture ResinEBI · Class 2 | Denture resins & teeth | Maker | Denture Base Resin(PN-Denture (Red,White)) | 2024 |
| Teeth Plastic DentureELM · Class 2 | Denture resins & teeth | Maker | Denture Base Resin(PN-Denture (Red,White)) | 2024 |
| Resin Denture Tooth Preformed Additively ManufacturedPZY · Class 2 | Denture resins & teeth | Maker | Denture Base Resin(PN-Denture (Red,White)) | 2024 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| SHENZHEN PIOCREAT 3D TECHNOLOGY CO., LTDFDA reg. 3022545323 | Shenzhen Guangdong, China | Foreign exporter, Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10087763). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.