DDS Lab China Co, LTD

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3009319807

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
3009319807
FEI Number
3009319807
Entity Name
DDS Lab China Co, LTD
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
5th Floor A01, D01, G01 4th Floor-B01, Gaoxinqi Factory Building, District 67, Xingdong Community, Xin'an Street, Baoan District, Shenzhen Guangdong 518100, 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
DDS Lab China Co, LTD (Owner Number: 10039165)
Owner / Operator Contact Address
5th Floor-A01, D01, G01; 4th Floor-B01, Gaoxinqi Factory Building,, District 67, Xingdong Community, Xin'an Street, Baoan District, Shenzhen, CN-GD 518100, 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
NSO Restoration, Porcelain-Fused-To-Metal Unknown Class N N/A 2011-12-14
NSP Restoration, Porcelain Unknown Class N N/A 2013-04-02
NSR Prosthesis, Orthodontic Unknown Class N N/A 2013-04-02
NSL Dentures, Full Unknown Class N N/A 2011-12-14
NSK Dentures, Partial Unknown Class N N/A 2011-12-14

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

DDS Lab China 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 3009319807. Last updated year: 2026. Please use registration number 3009319807 when referencing this establishment in official correspondence.
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