SHEN FU ARTS LAB

FDA Device Registration & Listing · Shen Zhen Guangdong, CN · Registration 3004578725

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
3004578725
FEI Number
3004578725
Entity Name
SHEN FU ARTS LAB
City/State/Country
Shen Zhen Guangdong, CN
Establishment Address
1F,12 Building, Xinxin tian Industrial Park, Xin Sha Road, Shajing Town, Shen Zhen Guangdong 518104, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SHEN FU ARTS LAB (Owner Number: 9063832)
Owner / Operator Contact Address
2/F, #B Bldg, Jin Xiu Rd. He-Yi Village, Shajing Town, Shen Zhen, CN-GD 518104, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EJH Alloy, Metal, Base Dental Class 2 872.3710 2007-11-08
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2016-12-15
NSO Restoration, Porcelain-Fused-To-Metal Unknown Class N N/A 2007-11-08
NSJ Restoration, Noble Metal Unknown Class N N/A 2010-06-11
NOF System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations Dental Class 2 872.3661 2010-06-11
EJS Alloy, Other Noble Metal Dental Class 2 872.3060 2007-11-08
EGD Wax, Dental, Intraoral Dental Class 1 872.6890 2010-06-11
NSQ Restoration, Base Metal Unknown Class N N/A 2010-06-11
NSR Prosthesis, Orthodontic Unknown Class N N/A 2007-11-08

Official Correspondent

No official correspondent registered.

US Agent Details

Amy Tsai Email: amy@rsulab.com Phone: (626) 2371218

Related Public Records

Same Entity

SHEN FU ARTS LAB
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K810521 C.Vaupel Dental, Inc. CO-SPAN 13.5 CASTING ALLOY 1981-03-17
K800400 Dentsply Intl. MAXUM DENTURE RESIN 1980-03-12
K033020 Cmp Industries, LLC IMPAK ACRYLIC REPAIR RESIN LIQUID 2003-12-19

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3039443707 SHANGHAI FRONTIER MATERIAL TECH CO., LTD. Shanghai, CN
2014676 The Belport Company, Inc DBA Gingi-Pak CAMARILLO, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004578725. Last updated year: 2026. Please use registration number 3004578725 when referencing this establishment in official correspondence.
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