MOLEX S.A. DE C.V.

FDA Device Registration & Listing · Nogales Sonora, MX · Registration 3013581838

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013581838
FEI Number
3013581838
Entity Name
MOLEX S.A. DE C.V.
City/State/Country
Nogales Sonora, MX
Establishment Address
Calzada Industrial Nuevo Nogales 1115, Nogales Sonora 84094, MX
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Molex S.A. de C.V. (Owner Number: 10090353)
Owner / Operator Contact Address
Calzada Industrial Nuevo Nogales 1115, Nogales, MX-SON 84094, MX
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LASSO 2515 V eco Variable Catheter and LASSO NAV Catheter TX eco EXT Cable Catheter, intracardiac mapping, high-density array

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2026-02-06
OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter Unknown Class 3 N/A 2024-03-15
MTD Catheter, Intracardiac Mapping, High-Density Array Cardiovascular Class 2 870.1220 2025-04-07

Official Correspondent

Arturo Montez

US Agent Details

TC Tan Email: tc.tan@molex.com Phone: (501) 8031165

Related Public Records

Same Entity

Molex S.A. de C.V.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K881966 C.R. Bard, Inc. ELECTROPHYSIOLOGY ELECTRODE CATH. W/SILVER/SILVER 1988-10-04
K192037 ABBOTT MEDICAL Advisor VL Circular Mapping Catheter, Sensor Enabled 2019-09-17
K241372 ABBOTT MEDICAL Advisor™ HD Grid X Mapping Catheter, Sensor Enabled™ 2024-07-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013581838. Last updated year: 2026. Please use registration number 3013581838 when referencing this establishment in official correspondence.
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