BENCHMARK ELECTRONICS San Jorge

FDA Device Registration & Listing · Tlajomulco de Zuniga Jalisco, MX · Registration 3037724692

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
3037724692
FEI Number
3037724692
Entity Name
BENCHMARK ELECTRONICS San Jorge
City/State/Country
Tlajomulco de Zuniga Jalisco, MX
Establishment Address
Circuito San Jorge 3538 Interior 9, Parque Industrial San Jorge, Tlajomulco de Zuniga Jalisco 45678, MX
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
BENCHMARK ELECTRONICS, INC. (Owner Number: 1641405)
Owner / Operator Contact Address
56 S Rockford Dr., --, Tempe, AZ 85288, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2026-03-25
DQK Computer, Diagnostic, Programmable Cardiovascular Class 2 870.1425 2026-03-25
QAQ Adjunctive Predictive Cardiovascular Indicator Cardiovascular Class 2 870.2210 2024-09-25
FLL Continuous Measurement Thermometer General Hospital Class 2 880.2910 2024-09-25
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2024-09-25
QMS Adjunctive Open Loop Fluid Therapy Recommender Cardiovascular Class 2 870.5600 2024-09-25
DSB Plethysmograph, Impedance Cardiovascular Class 2 870.2770 2024-09-25
DQK Computer, Diagnostic, Programmable Cardiovascular Class 2 870.1425 2024-09-25
DQE Catheter, Oximeter, Fiber-Optic Cardiovascular Class 2 870.1230 2024-09-25
MUD Oximeter, Tissue Saturation Cardiovascular Class 2 870.2700 2024-09-25

Official Correspondent

No official correspondent registered.

US Agent Details

Jeff Bovee Business: BENCHMARK ELECTRONICS, INC. Email: jeff.bovee@bench.com Phone: (602) 3333655

Related Public Records

Same Entity

BENCHMARK ELECTRONICS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3044741637 Benchmark Almelo Almelo Overijssel, NL
3003899230 BENCHMARK ELECTRONICS (THAILAND) PUBLIC COMPANY LI AYUDHAYA Phra Nakhon Si Ayutthaya, TH
2133641 BENCHMARK ELECTRONICS, INC. WINONA, MN, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K100940 Andon Health Co, Ltd. FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-5965 2010-06-29
K251581 Shenzhen Hingmed Medical Instrument Co., Ltd. Wearable Ambulatory Blood Pressure Monitor (WBP-02A) 2026-02-13
K200521 Health & Life Co., Ltd. Full Automatic(NIBP) Blood Pressure Monitor 2020-06-12
K152003 Andon Health Co, Ltd. iHealth BP3L Wireless Blood Pressure Monitor 2015-09-24
K952827 Sein Electronics Co., Ltd. FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000 1996-11-14

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0032-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Z-0033-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.
Z-0034-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.
Z-0002-2016 Biosense Webster, Inc. 2
Carto 3 EP Navigation System. Electro physiology system which views of the electrical activity of the heart through real-time data on 3-D, color-coded cardiac maps.
Z-0032-05 Siemens Medical Solutions USA, Inc 2
AXIOM Sensis Programmable diagnostic computer, Model number 66 23 974.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3037724692. Last updated year: 2026. Please use registration number 3037724692 when referencing this establishment in official correspondence.
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