Data / Medical devices / Mexico / Convertors de Mexico S. de R.L. de C.V

Convertors de Mexico S. de R.L. de C.V: FDA-registered device maker in Ciudad Juarez Chihuahua, Mexico, 4 510(k) clearances

Name: Convertors de Mexico S. de R.L. de C.V FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Convertors de Mexico S. de R.L. de C.V is registered with the FDA (registration 3018167761) in Ciudad Juarez Chihuahua, Mexico. It lists 13 device types. The FDA files 4 510(k) clearances under its listings, the newest dated December 15, 1997. Registered through 2027. FDA data exported November 3, 2026.

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FDA registration number: 3018167761
Address: Blvd. Independencia No. 2460 Lote Bravo, Ciudad Juarez Chihuahua, Mexico, 32695
Owner or operator: Cardinal Health 200, LLC (9028292)
Roles: Manufacturer, Repackager or relabeler
First device listed: January 8, 1993
Registered through: 2027

Devices it lists

Device	Product code	Class	Role	Source
Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass	DTL	2	Repackager or relabeler	accessdata.fda.gov
Anesthesia Breathing Circuit Kit (Adult & Pediatric)	OFP	1	Manufacturer	accessdata.fda.gov
Blood And Urine Collection Kit (Excludes Hiv Testing)	OIB	1	Manufacturer	accessdata.fda.gov
Catheter, Peritoneal	GBW	1	Repackager or relabeler	accessdata.fda.gov
Chemotherapy Spill Clean-Up Kit	PWT	1	Manufacturer	accessdata.fda.gov
Drape, Surgical, Exempt	PUI	2	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Drug	FRO	U	Repackager or relabeler	accessdata.fda.gov
Infant Heel Warmer (Chemical Heat Pack)	MPO	1	Repackager or relabeler	accessdata.fda.gov
Pack, Hot Or Cold, Disposable	IMD	1	Repackager or relabeler	accessdata.fda.gov
Pad, Alcohol, Device Disinfectant	LKB	U	Repackager or relabeler	accessdata.fda.gov
Toothbrush, Manual	EFW	1	Repackager or relabeler	accessdata.fda.gov
Tray, Surgical	LRP	1	Manufacturer	accessdata.fda.gov
Tubes, Gastrointestinal (And Accessories)	KNT	2	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
December 15, 1997	K973507	KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)	FRO	Substantially Equivalent for Some Indications	Kendall Healthcare Products Co. Div.Of Tyco Health	accessdata.fda.gov
June 6, 1996	K961154	BAXTER SODIUM ACETATE INFANT HEEL WARMER	MPO	Substantially Equivalent	Baxter Healthcare Corp	accessdata.fda.gov
July 13, 1982	K821906	CORPAK ENTERIC FEEDING TUBE W/GUIDE TIP	KNT	Substantially Equivalent	Corpak Medsystems	accessdata.fda.gov
January 23, 1979	K782095	STOPCOCKS, MANIFOLDS	DTL	Substantially Equivalent	Namic	accessdata.fda.gov

Compare with other makers

Updated December 15, 1997. 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.