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Data / Medical devices / Mexico / Martech Medical Products S. De RL. De CV.

Martech Medical Products S. De RL. De CV.: FDA-registered device maker in MEXICALI Baja California, Mexico, 3 510(k) clearances

Martech Medical Products S. De RL. De CV. is registered with the FDA (registration 3003915875) in MEXICALI Baja California, Mexico. It lists 54 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 18, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3003915875
Address
Calle Mercurio N 46 Parque Industrial Mexicali 1, MEXICALI Baja California, Mexico, C.P. 21210
Owner or operator
MARTECH MEDICAL PRODUCTS (2527072)
Roles
Complaint file establishment, Contract manufacturer, Manufacturer
First device listed
May 18, 2006
Registered through
2026
Brand names listed
"X" SERIES PD CATHETER, 1.9F VASCU-PICC® (PEDIATRICS) (DUROMETER 2363-80A), 10F PEDIATRIC ASH-SPLIT CATH XL, 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER, 18 Ga. Introducer Needle, 18 X 45 GW KIT, 2.6F VASCU-PICC (DUROMETER 2363-80A), 25G Huber Needle and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, A-V ShuntKNZ2Contract manufactureraccessdata.fda.gov
Accessories, CatheterKGZ1Contract manufactureraccessdata.fda.gov
Accessories, Catheter, G-UKNY2Contract manufactureraccessdata.fda.gov
Applicator, EntKCJ1Contract manufactureraccessdata.fda.gov
Aspiration Therapy SystemOYF3Contract manufactureraccessdata.fda.gov
Bandage, Liquid, Skin ProtectantNEC1Contract manufactureraccessdata.fda.gov
Blade, ScalpelGES1Contract manufactureraccessdata.fda.gov
Cannula, InjectionFGY1Contract manufactureraccessdata.fda.gov
Catheter, CholangiographyGBZ1Contract manufactureraccessdata.fda.gov
Catheter, Conduction, AnestheticBSO2Contract manufactureraccessdata.fda.gov
Catheter, FemoralLFK2Contract manufactureraccessdata.fda.gov
Catheter, Hemodialysis, ImplantedMSD2Contract manufactureraccessdata.fda.gov
Catheter, Hemodialysis, Non-ImplantedMPB2Contract manufactureraccessdata.fda.gov
Catheter, Hemodialysis, Triple Lumen, Non-ImplantedNIE2Contract manufactureraccessdata.fda.gov
Catheter, InfusionJCY1Contract manufactureraccessdata.fda.gov
Catheter, Intravascular, DiagnosticDQO2Contract manufactureraccessdata.fda.gov
Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS2Contract manufacturer, Manufactureraccessdata.fda.gov
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ2Contract manufactureraccessdata.fda.gov
Catheter, IrrigationGBX1Contract manufactureraccessdata.fda.gov
Catheter, NasopharyngealENW1Contract manufactureraccessdata.fda.gov
Catheter, PercutaneousDQY2Contract manufactureraccessdata.fda.gov
Catheter, PeritonealGBW1Contract manufactureraccessdata.fda.gov
Catheter, Peritoneal, Long-Term IndwellingFJS2Contract manufactureraccessdata.fda.gov
Catheter, SubclavianLFJ2Contract manufactureraccessdata.fda.gov
Catheter, Ureteral, Gastro-UrologyEYB2Contract manufactureraccessdata.fda.gov
Catheter, Ventricular, General & Plastic SurgeryGBS1Contract manufactureraccessdata.fda.gov
Catheters, Suction, TracheobronchialBSY1Contract manufactureraccessdata.fda.gov
Cystoscope And Accessories, Flexible/RigidFAJ2Contract manufactureraccessdata.fda.gov
Device, Intravascular Catheter SecurementKMK1Contract manufactureraccessdata.fda.gov
Dilator, Vessel, For Percutaneous CatheterizationDRE2Contract manufactureraccessdata.fda.gov
Endoscope, NeurologicalGWG2Contract manufactureraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Contract manufactureraccessdata.fda.gov
Graft, Vascular, Stainless Steel TunnelerMZY2Contract manufactureraccessdata.fda.gov
Guide, Needle, SurgicalGDF1Contract manufactureraccessdata.fda.gov
Injector And Syringe, AngiographicDXT2Contract manufactureraccessdata.fda.gov
Instrument, Manual, Specialized Obstetric-GynecologicKNA2Contract manufactureraccessdata.fda.gov
Instruments, Surgical, CardiovascularDWS1Contract manufactureraccessdata.fda.gov
Introducer, CatheterDYB2Contract manufactureraccessdata.fda.gov
Kit, Repair, Catheter, HemodialysisNFK2Contract manufactureraccessdata.fda.gov
Laparoscope, General & Plastic SurgeryGCJ2Contract manufactureraccessdata.fda.gov
Midline CatheterPND2Contract manufactureraccessdata.fda.gov
Needle, Hypodermic, Single LumenFMI2Contract manufactureraccessdata.fda.gov
Non-Coring (Huber) NeedlePTI2Complaint file establishment, Contract manufacturer, Manufactureraccessdata.fda.gov
Port & Catheter, Implanted, Subcutaneous, IntravascularLJT2Contract manufactureraccessdata.fda.gov
Set, Administration, IntravascularFPA2Complaint file establishment, Contract manufacturer, Manufactureraccessdata.fda.gov
Splint, Intranasal SeptalLYA1Contract manufactureraccessdata.fda.gov
Stent, UreteralFAD2Contract manufactureraccessdata.fda.gov
Stethoscope, Esophageal, With Electrical ConductorsBZT2Contract manufactureraccessdata.fda.gov
Suture, Nonabsorbable, Synthetic, PolyamideGAR2Contract manufactureraccessdata.fda.gov
Tissue Expander And AccessoriesLCJUContract manufactureraccessdata.fda.gov
Tube, Gastro-EnterostomyKGC2Contract manufactureraccessdata.fda.gov
Tubes, Gastrointestinal (And Accessories)KNT2Contract manufactureraccessdata.fda.gov
Ureteroscope And Accessories, Flexible/RigidFGB2Contract manufactureraccessdata.fda.gov
Wire, Guide, CatheterDQX2Contract manufactureraccessdata.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
September 18, 2026K25409525G Huber NeedlePTISubstantially EquivalentMartech Medical Productsaccessdata.fda.gov
August 16, 2013K1316876F X 60CM TRIPLE PRO-LINE CT BASIC IR SETLJSSubstantially EquivalentMedical Components, Inc.accessdata.fda.gov
November 24, 2009K093309PRO-LINE CT (BASIC TRAY) MODEL MR28036101LJSSubstantially EquivalentMedcomp ( Medical Components)accessdata.fda.gov

Compare with other makers

Updated September 18, 2026. 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.