Manufacturer registered with FDA
ZiYang Rayform Technology Co., Ltd
Ziyang City, China. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 3
- 510(k) clearances
- 0as applicant
- Markets registered in
- 212 registrations outside the US
- Establishments
- 1China
Registered in 2 markets
Where regulators' registries name ZiYang Rayform Technology Co., Ltd as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | ZiYang Rayform Technology Co., Ltd | 1 device types | — | Below |
| European Union | EUDAMED | Manufacturer | Ziyang Rayform Technology Co.,Ltd | 12 | — | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What ZiYang Rayform 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 Impression Tray MaterialEBH · Class 1 | Impression trays | Maker | Surgical Guide (RF-DB-04), Indirect Bonding Tray Resin (RF-IR-14), Model Resin (RF-ZX-03, RF-MI-2103, RF-MI-1101),Try In Resin (RF-TIR-16), Tray Resin (RF-TR-15), Gingiva Mask (RF-YY-10), Ortho Model Resin (RF-ZJ-01),Water Washable Model Resin (RF-ZJ-02), Soft Splint (RF-SS-13), Hard Splint (RF-HS-12) | 2025 |
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 |
|---|---|---|
| ZIYANG RAYFORM TECHNOLOGY CO., LTDFDA reg. 3038194591 | Ziyang City Sichuan, China | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10093034). 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.