Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014142650

FEI Number

3014142650

Entity Name

CBD DENTAL LAB, INC

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

7th Floors, Building AB, No.37, Shengping Road, Luo Zu Community, Shi Yan Town, Bao an Dist, Shenzhen Guangdong 518100, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CBD DENTAL LAB, INC (Owner Number: 10056294)

Owner / Operator Contact Address

2F Bldg 3 and 2F Bldg 2, Yuan Jin Factory, Huang Feng Ling Industrial area, Luo Zu Community, Shi Yan Town, Bao an Dist, Shenzhen, CN-GD 518100, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dynamic Abutment Solutions Dynamic Abutment Solutions Prosthesis, orthodontic Restoration, porcelain Restoration, porcelain-fused-to-metal Restoration, resin Restoration, base metal Dentures, full

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NHA	Abutment, Implant, Dental, Endosseous	Dental	Class 2	872.3630	2024-11-27
NHA	Abutment, Implant, Dental, Endosseous	Dental	Class 2	872.3630	2024-11-27
NSR	Prosthesis, Orthodontic	Unknown	Class N	N/A	2017-11-27
NSP	Restoration, Porcelain	Unknown	Class N	N/A	2017-11-27
NSO	Restoration, Porcelain-Fused-To-Metal	Unknown	Class N	N/A	2017-11-27
NSM	Restoration, Resin	Unknown	Class N	N/A	2017-11-27
NSQ	Restoration, Base Metal	Unknown	Class N	N/A	2017-11-27
NSL	Dentures, Full	Unknown	Class N	N/A	2017-11-27

Official Correspondent

Karry Cheng

US Agent Details

Christopher Pendry Business: Dental Alliance Group Email: c.pendry@thedentalalliancegroup.com Phone: (800) 3341746

Related Public Records

Same Entity

CBD DENTAL LAB, INC

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
K211871	Faico Medical, LLC	FAICO Dental Implant System and CAD/CAM Abutments	2021-11-18

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-2018	Implant Direct Sybron Manufacturing, LLC	2	Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.

Similar Registrations

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3011587077	JIANGSU TRAUSIM MEDICAL INSTRUMENT CO.,LTD.	Changzhou Jiangsu, CN
3012121192	DENTAL EVOLUTIONS, INC	Beverly Hills, CA, US
3031529635	TRATE UAB	Kaunas Kauno Apskritis, LT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014142650. Last updated year: 2026. Please use registration number 3014142650 when referencing this establishment in official correspondence.