Data / Medical devices / United States / Cintas Corporation

Cintas Corporation: FDA-registered device maker in Middletown, OH, United States, 3 510(k) clearances

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

Cintas Corporation is registered with the FDA (registration 1121142) in Middletown, OH, United States. It lists 26 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 3, 2012. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 1121142
Address: 3577 Yankee Road Suite B, Middletown, OH, United States, 45044
Owner or operator: CINTAS CORPORATION (10023747)
Roles: Manufacturer, Repackager or relabeler
First device listed: February 10, 2012
Registered through: 2026
Brand names listed: Adhesive Bandage, Adhesive Tape, Adhesive Tape and Bandage, Bloodborne Pathogens Kit, Burn Kit, Cintas First Aid Kit W/ Drug, Cintas First Aid Kit W/O Drugs, Cold Spray and more

Devices it lists

Device	Product code	Class	Role	Source
Applicator, Absorbent Tipped, Non-Sterile	KXF	1	Repackager or relabeler	accessdata.fda.gov
Applicator, Absorbent Tipped, Sterile	KXG	1	Repackager or relabeler	accessdata.fda.gov
Bandage, Elastic	FQM	1	Repackager or relabeler	accessdata.fda.gov
Bandage, Liquid	KMF	1	Repackager or relabeler	accessdata.fda.gov
Bedding, Disposable, Medical	KME	1	Repackager or relabeler	accessdata.fda.gov
Blood Borne Pathogen Response Kit	PWP	1	Manufacturer	accessdata.fda.gov
Burn Kit With Drug	OJI	N	Manufacturer	accessdata.fda.gov
Depressor, Tongue, Non-Surgical	FMA	1	Repackager or relabeler	accessdata.fda.gov
Dressing, Compression	MHW	1	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Hydrogel Without Drug And/Or Biologic	NAE	1	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Hydrophilic	NAC	1	Repackager or relabeler	accessdata.fda.gov
Fiber, Medical, Absorbent	FRL	1	Repackager or relabeler	accessdata.fda.gov
First Aid Kit With Drug	LRR	N	Manufacturer	accessdata.fda.gov
First Aid Kit Without Drug	OHO	1	Manufacturer	accessdata.fda.gov
Gauze / Sponge,Nonresorbable For External Use	NAB	1	Repackager or relabeler	accessdata.fda.gov
Pack, Hot Or Cold, Disposable	IMD	1	Repackager or relabeler	accessdata.fda.gov
Pad, Eye	HMP	1	Repackager or relabeler	accessdata.fda.gov
Polymer Patient Examination Glove	LZA	1	Repackager or relabeler	accessdata.fda.gov
Scalpel, One-Piece	GDX	1	Repackager or relabeler	accessdata.fda.gov
Shield, Protective, Personnel	KPY	1	Repackager or relabeler	accessdata.fda.gov
Strip, Temperature, Forehead, Liquid Crystal	KPD	2	Repackager or relabeler	accessdata.fda.gov
Tape And Bandage, Adhesive	KGX	1	Repackager or relabeler	accessdata.fda.gov
Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use	PYO	1	Repackager or relabeler	accessdata.fda.gov
Thermometer, Clinical Color Change	FQZ	1	Repackager or relabeler	accessdata.fda.gov
Tourniquet, Nonpneumatic	GAX	1	Repackager or relabeler	accessdata.fda.gov
Vapocoolant Device	MLY	U	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 3, 2012	K121526	POWER-FREE NITRILE PATIENT EXAMINATION GLOVES	LZA	Substantially Equivalent	Shandong Junchi Medical Products Co., Ltd.	accessdata.fda.gov
February 23, 2006	K050757	FLEX-AID LIQUID GEL BANDAGE AND DERMAFLEX GEL TISSUE ADHESIVE PROFESSIONAL LIQUID BANDAGE	KMF	Substantially Equivalent	Chemence Medical, Inc.	accessdata.fda.gov
June 10, 2005	K033720	ARI COLD SPRAY	MLY	Substantially Equivalent	Ari	accessdata.fda.gov

Compare with other makers

Updated August 3, 2012. 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.