Riton 3D Technology Co., Ltd

FDA Device Registration & Listing · Guangzhou Guangdong, CN · Registration 3027303702

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3027303702
FEI Number
3027303702
Entity Name
Riton 3D Technology Co., Ltd
City/State/Country
Guangzhou Guangdong, CN
Establishment Address
Building 2 Room C101, Hejing Road; Li Wan District, Guangzhou Guangdong 510385, CN
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Riton 3D Technology Co., Ltd (Owner Number: 10087560)
Owner / Operator Contact Address
Room C101, Building 2, No. 21, Hejing South Road, Liwan District, Guangzhou, CN-GD 510385, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Splint Model HS1-T Splint Model SS1-T Gingiva Mask Model G2-P Denture Teeth Model DT1-A1 Denture Teeth Model DT1-A3 Denture Teeth Model DT1-A2 Try-in Model TN1-A2 Casting Wax Resin Model C1-G

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMY Positioner, Tooth, Preformed Dental Class 1 872.5525 2025-06-26
NOK Material, External Aesthetic Restoration, No Adhesive General, Plastic Surgery Class 1 878.3800 2023-03-31
PZY Additively Manufactured, Preformed, Resin Denture Tooth Dental Class 2 872.3590 2023-03-31
EEA Plate, Base, Shellac Dental Class 1 872.6200 2025-06-23
EGD Wax, Dental, Intraoral Dental Class 1 872.6890 2024-06-06

Official Correspondent

huang huang

US Agent Details

Jason Zhou Email: ShamrockIE49@hotmail.com Phone: (626) 6325067

Related Public Records

Same Entity

Riton 3D Technology Co., Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027303702. Last updated year: 2026. Please use registration number 3027303702 when referencing this establishment in official correspondence.
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