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Data / Medical devices / Mexico / 3M Edumex, S.A De C.V

3M Edumex, S.A De C.V: FDA-registered device maker in CD. JUAREZ Chihuahua, Mexico, 1 510(k) clearance

3M Edumex, S.A De C.V is registered with the FDA (registration 9680284) in CD. JUAREZ Chihuahua, Mexico. It lists 28 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 4, 1991. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9680284
FEI number
3002809016
Address
Avenida Ramon Rivera Lara 6620 Parque Industrial Ramon Rivera Lara, CD. JUAREZ Chihuahua, Mexico, 32605
Owner or operator
3M COMPANY (2110898)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
December 15, 1992
Registered through
2026
Brand names listed
3M, 3M Surgical Masks, 3M Tie-On Surgical Mask, 3M™, BAG, INTESTINE, BANDAGE, ELASTIC, BEDDING, DISPOSABLE, MEDICAL, BINDER, ABDOMINAL and more

Devices it lists

DeviceProduct codeClassRoleSource
Bag, IntestineKGY1Contract manufactureraccessdata.fda.gov
Bandage, ElasticFQM1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Bedding, Disposable, MedicalKME1Contract manufactureraccessdata.fda.gov
Binder, AbdominalFSD1Manufactureraccessdata.fda.gov
Drape, Adhesive, AerosolKGT1Contract manufactureraccessdata.fda.gov
Drape, Surgical, AntimicrobialKKX2Contract manufactureraccessdata.fda.gov
Drape, Surgical, ExemptPUI2Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Drape, Urological, DisposableEYY2Contract manufactureraccessdata.fda.gov
Dressing, CompressionMHW1Repackager or relabeleraccessdata.fda.gov
Dressing, Wound, HydrophilicNAC1Repackager or relabeleraccessdata.fda.gov
Dressing, Wound, OcclusiveNAD1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Fiber, Medical, AbsorbentFRL1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Joint, Ankle, External BraceITW1Manufactureraccessdata.fda.gov
Joint, Knee, External BraceITQ1Manufactureraccessdata.fda.gov
Mask, SurgicalFXX2Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Orthosis, CervicalIQK1Manufactureraccessdata.fda.gov
Orthosis, Limb BraceIQI1Manufactureraccessdata.fda.gov
Orthosis, Truncal/Orthosis, LimbMRI1Manufactureraccessdata.fda.gov
Pack, Hot Or Cold, DisposableIMD1Repackager or relabeleraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Repackager or relabeleraccessdata.fda.gov
Pad, EyeHMP1Contract manufactureraccessdata.fda.gov
Ring (Wound Protector), Drape Retention, InternalKGW2Contract manufactureraccessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)HOY1Repackager or relabeleraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Manufactureraccessdata.fda.gov
Staple, Removable (Skin)GDT1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Support, ArmIOY1Manufactureraccessdata.fda.gov
System, Thermal RegulatingDWJ2Contract manufactureraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Manufacturer, Repackager or relabeleraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 4, 1991K9101823M BRAND EAR LOOP FACE MASK, 2000FFXXSubstantially Equivalent3M Companyaccessdata.fda.gov

Compare with other makers

Updated March 4, 1991. 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.