Data / Medical devices / China / CBD Dental Lab, Inc

CBD Dental Lab, Inc: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances

Name: CBD Dental Lab, Inc FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

CBD Dental Lab, Inc is registered with the FDA (registration 3014142650) in Shenzhen Guangdong, China. It lists 11 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 17, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3014142650
Address: 7th Floors, Building AB, No.37, Shengping Road, Luo Zu Community, Shi Yan Town Bao an Dist, Shenzhen Guangdong, China, 518100
Owner or operator: CBD DENTAL LAB, INC (10056294)
Roles: Manufacturer
First device listed: November 26, 2017
Registered through: 2026
Brand names listed: Dentures, full, Dentures, partial, Dynamic Abutment Solutions, Prosthesis, orthodontic, Restoration, base metal, Restoration, noble metal, Restoration, porcelain, Restoration, porcelain-fused-to-metal and more

Devices it lists

Device	Product code	Class	Role	Source
Abutment, Implant, Dental, Endosseous	NHA	2	Manufacturer	accessdata.fda.gov
Dentures, Full	NSL	N	Manufacturer	accessdata.fda.gov
Dentures, Partial	NSK	N	Manufacturer	accessdata.fda.gov
Prosthesis, Orthodontic	NSR	N	Manufacturer	accessdata.fda.gov
Restoration, Base Metal	NSQ	N	Manufacturer	accessdata.fda.gov
Restoration, Noble Metal	NSJ	N	Manufacturer	accessdata.fda.gov
Restoration, Porcelain	NSP	N	Manufacturer	accessdata.fda.gov
Restoration, Porcelain-Fused-To-Metal	NSO	N	Manufacturer	accessdata.fda.gov
Restoration, Resin	NSM	N	Manufacturer	accessdata.fda.gov
Restoration, Resin, Crown And Bridge	NSN	N	Manufacturer	accessdata.fda.gov
System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations	NOF	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
October 17, 2023	K232151	Dynamic TiBase	NHA	Substantially Equivalent	Talladium España, SL	accessdata.fda.gov
May 4, 2018	K162021	3.0 Dynamic TiBase	NHA	Substantially Equivalent	Talladium Espana, SL	accessdata.fda.gov

Compare with other makers

Updated October 17, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.