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Maytex Corp.

Last updated May 23, 2026

Information

Page 3 of 3

Device	Model / Reference	Registries	Class	Status
Maytex face mask	3125MM	FDA UDI	Class II	Active
Maytex Nupack	STP7513	FDA UDI	Class II	Active
Maytex	5885BKL	FDA UDI	Class I	Active
Maytex	3135BL	FDA UDI	Class II	Active
Maytex	5875VBS	FDA UDI	Class I	Active
Maytex	6200TXL	FDA UDI	Class I	Active
Maytex	5885BKM	FDA UDI	Class I	Active
Maytex	6200BXL	FDA UDI	Class I	Active
Maytex	6200WXS	FDA UDI	Class I	Active
Maytex	6200PPS	FDA UDI	Class I	Active
Maytex Nupack	STP2710	FDA UDI	Class II	Active
Choyce	5875CVBXL	FDA UDI	Class I	Active
Mizuho Osi	OSI5844-11	FDA UDI	Class II	Active
Maytex Nupack	STP29	FDA UDI	Class II	Active
Maytex	6250T-S	FDA UDI	Class I	Active
Maytex Nupack	STP225	FDA UDI	Class II	Active
Maytex	6200BL	FDA UDI	Class I	Active
Maytex	6200TXXL	FDA UDI	Class I	Active
Maytex Non-Sterile Latex Exam Gloves	K892082	FDA 510(k)	Class I	Active
Maytex Powder-Free Latex Examination Gloves	K935315	FDA 510(k)	Class I	Active
Maytex Latex Examination Gloves	K892183	FDA 510(k)	Class I	Active
Maytex Latex Examination Gloves, Powdered	K935314	FDA 510(k)	Class I	Active

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Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
May 15, 2013	Z-1451-2013	—	terminated	Recent Lab testing conducted in March 2013 indicates that the product does not meet the standard of "Differential Pressure of only 1.6 Delta P (mm H2O/cm2)" as indicated on the box/package of the product; and also product manufactured between 2008 - 2012 cannot be guaranteed as Fluid Resistant.