Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029906631

FEI Number

3029906631

Entity Name

VIA SYSTEMS MANUFACTURAS

City/State/Country

Tijuana Baja California, MX

Establishment Address

Blvd. Lic. Hector Teran Teran, Canon del Padre No. 20662 interior A, Colonia murua oriente, Tijuana Baja California 22203, MX

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Via systems Manufacturas (Owner Number: 10088793)

Owner / Operator Contact Address

Blvd. Lic. Hector Teran Teran, Canon del Padre No. 20662 interior A, Colonia murua oriente, Tijuana, MX-BCN 22203, MX

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PUREWAY COMPLIANCE, INC CONTIPI MEDICAL LTD Ortho-Clinical Diagnostics, Inc Ortho-Clinical Diagnostics, Inc

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2025-07-22
HHW	Pessary, Vaginal	Obstetrics/Gynecology	Class 2	884.3575	2023-10-11
PSZ	Devices Detecting Influenza A, B, And C Virus Antigens	Microbiology	Class 2	866.3328	2025-09-29
KHO	Fluorometer, For Clinical Use	Clinical Chemistry	Class 1	862.2560	2025-09-29
GQG	Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus	Microbiology	Class 1	866.3480	2025-09-29

Official Correspondent

cesar Salas

US Agent Details

KEVIN AHERN Business: SPLAY Email: kahern@ksplastic.com Phone: (510) 3518230

Related Public Records

Same Entity

Via systems Manufacturas

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
K933654	Johnson & Johnson Medical, Inc.	BLADDER NECK SUPPORT PROTHESIS FITTING KIT	1995-05-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029906631. Last updated year: 2026. Please use registration number 3029906631 when referencing this establishment in official correspondence.