Data / Medical devices / Mexico / Conamco SA de CV Medental Inc

Conamco SA de CV Medental Inc: FDA-registered device maker in C.P. 06880 Ciudad de Mexico, Mexico, 7 510(k) clearances

Name: Conamco SA de CV Medental Inc FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Conamco SA de CV Medental Inc is registered with the FDA (registration 3006805063) in C.P. 06880 Ciudad de Mexico, Mexico. It lists 7 device types. The FDA files 7 510(k) clearances under its listings, the newest dated April 2, 1999. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3006805063
Address: Jose Maria Bustillos No. 28 Bis, 1er y 2do piso. Colonia Algarin, Delegacion Cuauhtemoc, C.P. 06880 Ciudad de Mexico, Mexico, 06880
Owner or operator: Conamco (10038806)
Roles: Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed: November 14, 2011
Registered through: 2026
Brand names listed: Crushed Quartz, Medental, Medental Prophy Paste

Devices it lists

Device	Product code	Class	Role	Source
Adhesive, Bracket And Tooth Conditioner, Resin	DYH	2	Contract manufacturer	accessdata.fda.gov
Agent, Polishing, Abrasive, Oral Cavity	EJR	1	Manufacturer	accessdata.fda.gov
Cement, Dental	EMA	2	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Material, Tooth Shade, Resin	EBF	2	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Sealant, Pit And Fissure, And Conditioner	EBC	2	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Varnish, Cavity	LBH	2	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Zinc Oxide Eugenol	EMB	1	Contract manufacturer, Manufacturer, 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
April 2, 1999	K990314	MULTI-CURE COMPOSITE CEMENT	EBF	Substantially Equivalent	Medental Intl.	accessdata.fda.gov
October 22, 1998	K983018	ZINC PHOSPHATE CEMENT	EMA	Substantially Equivalent	Medental Intl.	accessdata.fda.gov
September 30, 1998	K982779	MEDENTAL GLASS IONOMER CEMENT TYPE I AND MIRAGE GLASS IONOMER CEMENT TYPE 1	EMA	Substantially Equivalent	Medental Intl.	accessdata.fda.gov
September 14, 1998	K982191	CHEMICAL CURE COMPOSITE WITH ENAMEL BOND	EBF	Substantially Equivalent	Medental Intl.	accessdata.fda.gov
July 31, 1998	K980990	POLYCARBOXYLATE CEMENT	EMA	Substantially Equivalent	Medental Intl.	accessdata.fda.gov
December 16, 1997	K973919	CAVITY VARNISH (INTERMEDIARY VARNISH AND DENTINAL TUBULI SEAL)	LBH	Substantially Equivalent	Medental Intl.	accessdata.fda.gov
November 25, 1997	K973541	MEDENTAL CHEMICAL CURING SEALANT PIT & FISSURE TINTED	EBC	Substantially Equivalent	Medental Intl.	accessdata.fda.gov

Compare with other makers

Updated April 2, 1999. 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.