Data / Medical devices / United States / Cordica Medical, Inc.

Cordica Medical, Inc.: FDA-registered device maker in Morristown, TN, United States, 3 510(k) clearances

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

Cordica Medical, Inc. is registered with the FDA (registration 1051594) in Morristown, TN, United States. It lists 31 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 17, 2010. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 1051594
Address: 6006 Superior Ct, Morristown, TN, United States, 37814
Owner or operator: Cordica Medical (Formally Team Technologies, Inc) (1051594)
Roles: Complaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer
First device listed: April 8, 1998
Registered through: 2027
Brand names listed: AllPro Interdentals, CVS Tongue Cleaner, Child Resistant Topi-CLICK, Colgate Adv Optic White, Dr. Fresh Reach, Interdentals - Various Colors, MOUTH MIRROR, Mident Dental Trays and more

Devices it lists

Device	Product code	Class	Role	Source
Agent, Polishing, Abrasive, Oral Cavity	EJR	1	Repackager or relabeler	accessdata.fda.gov
Alarm, Conditioned Response Enuresis	KPN	2	Contract manufacturer	accessdata.fda.gov
Applicator, Absorbent Tipped, Non-Sterile	KXF	1	Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer	accessdata.fda.gov
Applicator, Resin	KXR	1	Manufacturer	accessdata.fda.gov
Applicator, Vaginal	HGD	1	Complaint file establishment, Manufacturer	accessdata.fda.gov
Brush, Scrub, Operating-Room	GEC	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Catheter And Tip, Suction	JOL	2	Contract manufacturer, Repackager or relabeler	accessdata.fda.gov
Cup, Prophylaxis	EHK	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Dental Hygiene Kit	NXZ	1	Contract manufacturer	accessdata.fda.gov
Detectors And Removers, Lice, (Including Combs)	LJL	1	Contract manufacturer	accessdata.fda.gov
Dispenser, Liquid Medication	KYX	1	Manufacturer	accessdata.fda.gov
Dispenser, Solid Medication	NXB	1	Complaint file establishment	accessdata.fda.gov
Eraser, Dental Stain	MAU	1	Repackager or relabeler	accessdata.fda.gov
Floss, Dental	JES	1	Contract manufacturer	accessdata.fda.gov
Handpiece, Contra- And Right-Angle Attachment, Dental	EGS	1	Complaint file establishment, Contract manufacturer	accessdata.fda.gov
Heat Source For Bleaching Teeth	EEG	1	Repackager or relabeler	accessdata.fda.gov
Instruments, Dental Hand	DZN	1	Repackager or relabeler	accessdata.fda.gov
Kit, Test, Pregnancy, Hcg, Over The Counter	LCX	2	Contract manufacturer	accessdata.fda.gov
Mirror, Mouth	EAX	1	Repackager or relabeler	accessdata.fda.gov
Mouthpiece, Saliva Ejector	DYN	1	Contract manufacturer	accessdata.fda.gov
Oral Surgery Tray	PWL	1	Complaint file establishment, Specification developer	accessdata.fda.gov
Patient Personal Hygiene Kit	NSB	1	Contract manufacturer	accessdata.fda.gov
Pick, Massaging	JET	1	Repackager or relabeler	accessdata.fda.gov
Scraper, Tongue	LCN	1	Contract manufacturer	accessdata.fda.gov
Spatula, Cervical, Cytological	HHT	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Test, Luteinizing Hormone (Lh), Over The Counter	NGE	1	Contract manufacturer	accessdata.fda.gov
Tip, Rubber, Oral Hygiene	JEW	1	Specification developer	accessdata.fda.gov
Toothbrush, Manual	EFW	1	Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer	accessdata.fda.gov
Toothbrush, Powered	JEQ	1	Contract manufacturer	accessdata.fda.gov
Varnish, Cavity	LBH	2	Contract manufacturer	accessdata.fda.gov
Wax, Dental, Intraoral	EGD	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
June 17, 2010	K100539	PREVENTECH PROPHYLAXIS PASTE WITH FLUORIDE	EJR	Substantially Equivalent	Preventive Technologies, Inc.	accessdata.fda.gov
July 24, 1997	K971849	CYTOLOGY BRUSH	HHT	Substantially Equivalent	Team Technologies, Inc.	accessdata.fda.gov
May 16, 1994	K941189	DISPOSABLE PROPHYLAXIS ANGLE	EGS	Substantially Equivalent	Team Technologies, Inc.	accessdata.fda.gov

Compare with other makers

Updated June 17, 2010. 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.