Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005621362

FEI Number

3005621362

Entity Name

Shanghai dental labs INC.

City/State/Country

SHANGHAI, CN

Establishment Address

F5 No.33 Xiya Road, PUDONG NEW AREA, SHANGHAI 200131, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Shanghai dental labs INC. (Owner Number: 9083819)

Owner / Operator Contact Address

F5 No.33 Xiya Road,, PUDONG NEW AREA, SHANGHAI, CN-NOTA 200131, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Orthodontic appliance and accessories Backing and facing for an artificial tooth Preformed gold denture tooth

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DYJ	Retainer, Screw Expansion, Orthodontic	Dental	Class 1	872.5410	2013-01-12
ELK	Teeth, Artificial, Backing And Facing	Dental	Class 1	872.3910	2006-03-06
ELN	Teeth, Preformed Gold Denture	Dental	Class 1	872.3580	2006-03-06

Official Correspondent

Peilong Ma

US Agent Details

James H. Liao Email: james@sino2us.com Phone: (310) 3758169

Related Public Records

Same Entity

Shanghai dental labs INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3017092365	APNOMED, INC.	Bellevue, WA, US
1000385618	LEWA-DENTAL GMBH & CO. KG	REMCHINGEN Baden-Wurttemberg, DE
3009687180	KTJ DENTAL LAB COMPANY LIMITED	KL, HK
3015337428	GUANGZHOU CHEER-U MATERIAL TECHNOLOGY CO., LTD	Guangzhou Guangdong, CN
3024749697	SPRINTRAY INC.	Huntington Beach, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005621362. Last updated year: 2026. Please use registration number 3005621362 when referencing this establishment in official correspondence.