Data / Medical devices / United States / T D Dental Supply,inc

T D Dental Supply,inc: FDA-registered device maker in Santa Fe Springs, CA, United States, 6 510(k) clearances

Name: T D Dental Supply,inc FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

T D Dental Supply,inc is registered with the FDA (registration 3008792854) in Santa Fe Springs, CA, United States. It lists 8 device types. The FDA files 6 510(k) clearances under its listings, the newest dated August 27, 2014. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3008792854
Address: 8541 Wellsford PL. Suite E, Santa Fe Springs, CA, United States, 90670
Owner or operator: TD Dental Supply, Inc. (10034289)
Roles: Repackager or relabeler
First device listed: November 19, 2010
Registered through: 2026
Brand names listed: KAITONG/ROYAL SYNTHETIC POLYMER TEETH, RIZHAO HUGE DENTLA INDUSTRY COMPANY, LIMITED, Upcera Zirconia Block

Devices it lists

Device	Product code	Class	Role	Source
Alloy, Metal, Base	EJH	2	Repackager or relabeler	accessdata.fda.gov
Bur, Dental	EJL	1	Repackager or relabeler	accessdata.fda.gov
Denture, Plastic, Teeth	ELM	2	Repackager or relabeler	accessdata.fda.gov
Material, Impression	ELW	2	Repackager or relabeler	accessdata.fda.gov
Powder, Porcelain	EIH	2	Repackager or relabeler	accessdata.fda.gov
System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations	NOF	2	Repackager or relabeler	accessdata.fda.gov
Teeth, Porcelain	ELL	2	Repackager or relabeler	accessdata.fda.gov
Tray, Impression, Preformed	EHY	1	Repackager or relabeler	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
August 27, 2014	K141162	ALL-CERAMIC ZIRCONIA BLOCK	EIH	Substantially Equivalent	Rizhao Huge Dental Industry Co., Ltd.	accessdata.fda.gov
May 28, 2014	K133071	ELASTIC IMPRESSION MATERIAL	ELW	Substantially Equivalent	Rizhao Huge Dental Industry Co., Ltd.	accessdata.fda.gov
July 20, 2011	K111291	AIDITE ZIRCONIA DENTAL CERAMICS	EIH	Substantially Equivalent	Qinhuangdao Aidite High-Technical Ceramics Co, Ltd.	accessdata.fda.gov
August 16, 2010	K101029	KAIFENG/CRYSTAL, KAILI, KAIJING, KAIYUE, MAIST AND KAITONG/ROYAL SYNTHETIC POLYMER TEETH	ELM	Substantially Equivalent	Huge Dental Material Co., Ltd.	accessdata.fda.gov
January 28, 2010	K093560	UPCERA ZIRCONIA BLANKS	EIH	Substantially Equivalent	Shenyang Upcera Co., Ltd.	accessdata.fda.gov
October 25, 1991	K913372	IPS EMPRESS	EIH	Substantially Equivalent	Ivoclar North America, Inc.	accessdata.fda.gov

Compare with other makers

Updated August 27, 2014. 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.