Data / Medical devices / Mexico / Medline Soluciones Medicas
Medline Soluciones Medicas: FDA-registered device maker in Nuevo Laredo Tamaulipas, Mexico, 2 510(k) clearances
Medline Soluciones Medicas is registered with the FDA (registration 3045816902) in Nuevo Laredo Tamaulipas, Mexico. It lists 77 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 16, 1993. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3045816902
- Address
- New York 303 Parque Industrial Oradel, Nuevo Laredo Tamaulipas, Mexico, 88285
- Owner or operator
- Medline Industries, LP (1417592)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- December 29, 1977
- Registered through
- 2026
- Brand names listed
- 140928-Suture Removal Kit CSTM, 145666-Dressing Change CSTM, 147572-Sterile Circumcision Tray CSTM, 171415-O.R. KIT CSTM, 321236-Sterile Biospy CSTM, 946240-Skin Prep CSTM, ACCU-SORB, AKTORmed and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Accessories, Catheter | KGZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass | DTL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Anesthesia Breathing Circuit Kit (Adult & Pediatric) | OFP | 1 | Manufacturer | accessdata.fda.gov |
| Angiography/Angioplasty Kit | OEQ | 2 | Manufacturer | accessdata.fda.gov |
| Bag, Reservoir | BTC | 1 | Manufacturer | accessdata.fda.gov |
| Bandage, Elastic | FQM | 1 | Manufacturer | accessdata.fda.gov |
| Basin, Emesis | FNY | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Blood And Urine Collection Kit (Excludes Hiv Testing) | OIB | 1 | Manufacturer | accessdata.fda.gov |
| Body Fluid Clean Up Kit | OKG | 2 | Manufacturer | accessdata.fda.gov |
| Burn Kit Without Drug | OJJ | 1 | Manufacturer | accessdata.fda.gov |
| Cardiac Catheterization Kit | OES | 2 | Manufacturer | accessdata.fda.gov |
| Cardiovascular Procedure Kit | OEZ | 2 | Manufacturer | accessdata.fda.gov |
| Catheter And Tip, Suction | JOL | 2 | Manufacturer | accessdata.fda.gov |
| Catheter Care Tray | OHR | 2 | Manufacturer | accessdata.fda.gov |
| Catheter Introducer Kit | OFD | 2 | Manufacturer | accessdata.fda.gov |
| Central Venous Catheter Dressing Change Kit | PEZ | 2 | Manufacturer | accessdata.fda.gov |
| Central Venous Catheter Tray | OFF | 2 | Manufacturer | accessdata.fda.gov |
| Cesarean Section Tray | OHM | 2 | Manufacturer | accessdata.fda.gov |
| Chemotherapy Spill Clean-Up Kit | PWT | 1 | Manufacturer | accessdata.fda.gov |
| Chest Drainage Kit | PAD | 2 | Manufacturer | accessdata.fda.gov |
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Manufacturer | accessdata.fda.gov |
| Circumcision Tray | OHG | 2 | Manufacturer | accessdata.fda.gov |
| Container, Liquid Medication, Graduated | KYW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Container, Specimen, Sterile | FMH | 1 | Manufacturer | accessdata.fda.gov |
| Cover, Limb | IPM | 1 | Manufacturer | accessdata.fda.gov |
| Ct Biopsy Tray | OFG | 2 | Manufacturer | accessdata.fda.gov |
| Dialysis Administration Kit | PEV | 2 | Manufacturer | accessdata.fda.gov |
| Drape, Surgical, Exempt | PUI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Dress, Surgical | FYE | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Dressing Change Tray | OXQ | 1 | Manufacturer | accessdata.fda.gov |
| Ear, Nose, And Throat Surgical Tray | OGR | 1 | Manufacturer | accessdata.fda.gov |
| Endoscope Introducer Kit | NWU | 2 | Manufacturer | accessdata.fda.gov |
| Epidural Anesthesia Kit | OGE | 2 | Manufacturer | accessdata.fda.gov |
| Eye Tray | OJK | 2 | Manufacturer | accessdata.fda.gov |
| Filter, Bacterial, Breathing-Circuit | CAH | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Foley Catheter Kit (Excludes Hiv Testing) | PPB | 2 | Manufacturer | accessdata.fda.gov |
| Forceps | HTD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Forceps, General & Plastic Surgery | GEN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Gauze/Sponge, Internal, X-Ray Detectable | GDY | 1 | Repackager or relabeler | accessdata.fda.gov |
| General Purpose Dental Tray | OFX | 1 | Manufacturer | accessdata.fda.gov |
| General Surgery Tray | LRO | 2 | Manufacturer | accessdata.fda.gov |
| Gynecological Laparoscopic Kit | OHD | 2 | Manufacturer | accessdata.fda.gov |
| Hemostat | HRQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hysterectomy Kit | OJF | 2 | Manufacturer | accessdata.fda.gov |
| I.V. Start Kit | LRS | 2 | Manufacturer | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Kit, Surgical Instrument, Disposable | KDD | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Label Or Tag, Sterile | LYV | 1 | Manufacturer | accessdata.fda.gov |
| Labor And Delivery Kit | MLS | 2 | Manufacturer | accessdata.fda.gov |
| Laceration Tray | PKD | 1 | Manufacturer | accessdata.fda.gov |
| Laparoscopy Kit | FDE | 2 | Manufacturer | accessdata.fda.gov |
| Mixer, Breathing Gases, Anesthesia Inhalation | BZR | 2 | Manufacturer | accessdata.fda.gov |
| Nerve Block Tray | OGJ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Neurological Tray | OJG | 1 | Manufacturer | accessdata.fda.gov |
| Obstetrical Kit | OKV | 2 | Manufacturer | accessdata.fda.gov |
| Operating Room Accessories Table Tray | FWZ | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Orthopedic Tray | OJH | 1 | Manufacturer | accessdata.fda.gov |
| Patient Personal Hygiene Kit | NSB | 1 | Manufacturer | accessdata.fda.gov |
| Pelvic Exam Kit | MLT | 2 | Manufacturer | accessdata.fda.gov |
| Plastic Surgery And Accessories Kit | FTN | 1 | Manufacturer | accessdata.fda.gov |
| Razor, Surgical | LWK | 1 | Manufacturer | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Skin Prep Tray | OJU | 1 | Manufacturer | accessdata.fda.gov |
| Spinal Epidural Anesthesia Kit | OFT | 2 | Manufacturer | accessdata.fda.gov |
| Suture Removal Kit | MCZ | 1 | Manufacturer | accessdata.fda.gov |
| Tracheobronchial Suction Catheter Kit | OFR | 1 | Manufacturer | accessdata.fda.gov |
| Tracheostomy Cleaning Tray | OGV | 2 | Manufacturer | accessdata.fda.gov |
| Tracheotomy Care Kit | NXA | 2 | Manufacturer | accessdata.fda.gov |
| Tray, Biopsy, Without Biopsy Instruments | FCH | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) | FCM | 2 | Manufacturer | accessdata.fda.gov |
| Tray, Irrigation, Sterile | EYN | 2 | Manufacturer | accessdata.fda.gov |
| Tray, Surgical, Ent | MMO | 1 | Manufacturer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Urinal | FNP | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Wound Dressing Kit | MCY | 2 | 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 16, 1993 | K925591 | MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST | BZR | Substantially Equivalent | Merit Medical Systems, Inc. | accessdata.fda.gov |
| January 26, 1993 | K925217 | MERIDIAN MEDICAL SYSTEMS BREATHING FILTER | CAH | Substantially Equivalent | Merit Medical Systems, Inc. | accessdata.fda.gov |
Compare with other makers
Updated September 16, 1993. 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.