MG MEDICAL PRODUCTS LLC

FDA Device Registration & Listing · Cincinnati, OH, US · Registration 3018044766

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
3018044766
FEI Number
3018044766
Entity Name
MG MEDICAL PRODUCTS LLC
City/State/Country
Cincinnati, OH, US
Establishment Address
1095 Nimitzview Drive, Suite 101, Cincinnati, OH 45230, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MG Medical Products LLC (Owner Number: 10080993)
Owner / Operator Contact Address
1095 Nimitzview Drive, Suite 101, Cincinnati, OH 45230, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EKG Patch EKG Patch Solution Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRX Electrode, Electrocardiograph Cardiovascular Class 2 870.2360 2021-08-12
OEZ Cardiovascular Procedure Kit Cardiovascular Class 2 870.1200 2024-12-10

Official Correspondent

Jeffrey McGrath

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MG Medical Products LLC
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
K934333 3M Medical Products Group 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE 1994-07-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018044766. Last updated year: 2026. Please use registration number 3018044766 when referencing this establishment in official correspondence.
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