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
| Device | Product code | Class | Role | Source |
|---|
| Accessories, A-V Shunt | KNZ | 2 | Contract manufacturer | accessdata.fda.gov |
| Accessories, Catheter | KGZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Accessories, Catheter, G-U | KNY | 2 | Contract manufacturer | accessdata.fda.gov |
| Applicator, Ent | KCJ | 1 | Contract manufacturer | accessdata.fda.gov |
| Aspiration Therapy System | OYF | 3 | Contract manufacturer | accessdata.fda.gov |
| Bandage, Liquid, Skin Protectant | NEC | 1 | Contract manufacturer | accessdata.fda.gov |
| Blade, Scalpel | GES | 1 | Contract manufacturer | accessdata.fda.gov |
| Cannula, Injection | FGY | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Cholangiography | GBZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Conduction, Anesthetic | BSO | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Femoral | LFK | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Hemodialysis, Implanted | MSD | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Hemodialysis, Non-Implanted | MPB | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Hemodialysis, Triple Lumen, Non-Implanted | NIE | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Infusion | JCY | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Intravascular, Diagnostic | DQO | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days | LJS | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FOZ | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Irrigation | GBX | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Nasopharyngeal | ENW | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Percutaneous | DQY | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Peritoneal | GBW | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Peritoneal, Long-Term Indwelling | FJS | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Subclavian | LFJ | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Ureteral, Gastro-Urology | EYB | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Ventricular, General & Plastic Surgery | GBS | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Contract manufacturer | accessdata.fda.gov |
| Cystoscope And Accessories, Flexible/Rigid | FAJ | 2 | Contract manufacturer | accessdata.fda.gov |
| Device, Intravascular Catheter Securement | KMK | 1 | Contract manufacturer | accessdata.fda.gov |
| Dilator, Vessel, For Percutaneous Catheterization | DRE | 2 | Contract manufacturer | accessdata.fda.gov |
| Endoscope, Neurological | GWG | 2 | Contract manufacturer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Contract manufacturer | accessdata.fda.gov |
| Graft, Vascular, Stainless Steel Tunneler | MZY | 2 | Contract manufacturer | accessdata.fda.gov |
| Guide, Needle, Surgical | GDF | 1 | Contract manufacturer | accessdata.fda.gov |
| Injector And Syringe, Angiographic | DXT | 2 | Contract manufacturer | accessdata.fda.gov |
| Instrument, Manual, Specialized Obstetric-Gynecologic | KNA | 2 | Contract manufacturer | accessdata.fda.gov |
| Instruments, Surgical, Cardiovascular | DWS | 1 | Contract manufacturer | accessdata.fda.gov |
| Introducer, Catheter | DYB | 2 | Contract manufacturer | accessdata.fda.gov |
| Kit, Repair, Catheter, Hemodialysis | NFK | 2 | Contract manufacturer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Contract manufacturer | accessdata.fda.gov |
| Midline Catheter | PND | 2 | Contract manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Contract manufacturer | accessdata.fda.gov |
| Non-Coring (Huber) Needle | PTI | 2 | Complaint file establishment, Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Port & Catheter, Implanted, Subcutaneous, Intravascular | LJT | 2 | Contract manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Complaint file establishment, Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Splint, Intranasal Septal | LYA | 1 | Contract manufacturer | accessdata.fda.gov |
| Stent, Ureteral | FAD | 2 | Contract manufacturer | accessdata.fda.gov |
| Stethoscope, Esophageal, With Electrical Conductors | BZT | 2 | Contract manufacturer | accessdata.fda.gov |
| Suture, Nonabsorbable, Synthetic, Polyamide | GAR | 2 | Contract manufacturer | accessdata.fda.gov |
| Tissue Expander And Accessories | LCJ | U | Contract manufacturer | accessdata.fda.gov |
| Tube, Gastro-Enterostomy | KGC | 2 | Contract manufacturer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 2 | Contract manufacturer | accessdata.fda.gov |
| Ureteroscope And Accessories, Flexible/Rigid | FGB | 2 | Contract manufacturer | accessdata.fda.gov |
| Wire, Guide, Catheter | DQX | 2 | Contract manufacturer | 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 |
|---|
| September 18, 2026 | K254095 | 25G Huber Needle | PTI | Substantially Equivalent | Martech Medical Products | accessdata.fda.gov |
| August 16, 2013 | K131687 | 6F X 60CM TRIPLE PRO-LINE CT BASIC IR SET | LJS | Substantially Equivalent | Medical Components, Inc. | accessdata.fda.gov |
| November 24, 2009 | K093309 | PRO-LINE CT (BASIC TRAY) MODEL MR28036101 | LJS | Substantially Equivalent | Medcomp ( Medical Components) | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- All makers of Catheter, Percutaneous
- All makers of Port & Catheter, Implanted, Subcutaneous, Intravascular
- All makers of Catheter, Hemodialysis, Implanted
- All makers of Ureteroscope And Accessories, Flexible/Rigid
- All makers of Catheter, Subclavian
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.