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Data / Medical devices / Mexico / BSN Medical S.A. de C.V.

BSN Medical S.A. de C.V.: FDA-registered device maker in Reynosa Tamaulipas, Mexico, 2 510(k) clearances

BSN Medical S.A. de C.V. is registered with the FDA (registration 9612388) in Reynosa Tamaulipas, Mexico. It lists 26 device types. The FDA files 2 510(k) clearances under its listings, the newest dated August 20, 1999. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9612388
FEI number
3003255844
Address
Av. del Parque SN Villa Florida, Reynosa Tamaulipas, Mexico, 88715
Owner or operator
BSN medical GmbH (9047426)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
December 27, 1983
Registered through
2026
Brand names listed
, Jobst Comprifore #2, ACTIMOVE, ACTIMOVE KIDS ELBOW SUPPORT, ADJUSTABLE, ACTIMOVE KIDS WRIST STABILIZER, REMOVABLE METAL STAY, LEFT OR RIGHT, ACTIMOVE POST-OP ROM KNEE BRACE, ACTIMOVE PROFESSIONAL LINE MANUS, WRIST STABILIZER, ACTIMOVE SOLEA, Actimove Alufoam and more

Devices it lists

DeviceProduct codeClassRoleSource
Band Or Belt, Pelvic SupportISR1Manufactureraccessdata.fda.gov
Bandage, CastITG1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Bandage, ElasticFQM1Manufactureraccessdata.fda.gov
Binder, BreastHEF1Manufactureraccessdata.fda.gov
Binder, Medical, TherapeuticMDR1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Component, CastLGF1Manufactureraccessdata.fda.gov
Joint, Ankle, External BraceITW1Manufactureraccessdata.fda.gov
Joint, Knee, External BraceITQ1Manufactureraccessdata.fda.gov
Orthosis, AbdominalKTD1Manufactureraccessdata.fda.gov
Orthosis, CervicalIQK1Manufactureraccessdata.fda.gov
Orthosis, Corrective ShoeKNP1Repackager or relabeleraccessdata.fda.gov
Orthosis, Limb BraceIQI1Manufactureraccessdata.fda.gov
Orthosis, LumbarIQE1Manufactureraccessdata.fda.gov
Orthosis, Lumbo-SacralIPY1Manufactureraccessdata.fda.gov
Orthosis, Rib Fracture, SoftIPX1Manufactureraccessdata.fda.gov
Orthosis, Truncal/Orthosis, LimbMRI1Manufactureraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Repackager or relabeleraccessdata.fda.gov
Sling, ArmILI1Manufactureraccessdata.fda.gov
Splint, ClavicleIQJ1Manufactureraccessdata.fda.gov
Splint, Extremity, Non-Inflatable, External, Non-SterileNOC1Manufactureraccessdata.fda.gov
Splint, Extremity, Noninflatable, External, SterileFYH1Manufactureraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Manufactureraccessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)FQL1Manufactureraccessdata.fda.gov
Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)DWL2Contract manufacturer, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Support, ArmIOY1Manufactureraccessdata.fda.gov
Support, HerniaEXN1Manufactureraccessdata.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
August 20, 1999K991570JOBST READY-TO-WEAR ARM SLEEVESDWLSubstantially EquivalentBeiersdorf-Jobt, Inc.accessdata.fda.gov
May 18, 1995K951234MEDICAL SUPPORT STOCKINGSDWLSubstantially EquivalentJobst A Beiersdorf Co.accessdata.fda.gov

Compare with other makers

Updated August 20, 1999. 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.