WR MEDICAL ELECTRONICS CO.

FDA Device Registration & Listing · Maplewood, MN, US · Registration 2118418

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
2118418
FEI Number
2118418
Entity Name
WR MEDICAL ELECTRONICS CO.
City/State/Country
Maplewood, MN, US
Establishment Address
1700 Gervais Ave, Maplewood, MN 55109, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
WR MEDICAL ELECTRONICS CO. (Owner Number: 2118418)
Owner / Operator Contact Address
1700 GERVAIS AVE, --, Maplewood, MN 55109, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Meridian QSweat HRV Acquire Iontophor Iontophor CASEIV Therabath

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EGJ Device, Iontophoresis, Other Uses Physical Medicine Class 2 890.5525 2007-11-09
KTB Device, Iontophoresis, Specific Uses Physical Medicine Class 2 890.5525 2007-11-09
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) Cardiovascular Class 2 870.2300 2012-11-01
EGJ Device, Iontophoresis, Other Uses Physical Medicine Class 2 890.5525 2013-11-27
EGJ Device, Iontophoresis, Other Uses Physical Medicine Class 2 890.5525 2013-11-27
LLN Device, Vibration Threshold Measurement Neurology Class 1 882.1200 2007-11-09
IMC Bath, Paraffin Physical Medicine Class 2 890.5110 2007-11-09

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WR MEDICAL ELECTRONICS CO.
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
K842483 Santa Barbara Medco, Inc. SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC 1984-08-31
K832250 Litton Medical Electronics SERVOMED BASIC BEDSIDE UNIT SMA 102- 1984-06-01
K801515 Abbott Medical Electronics Co. ABBY II PATIENT MONITOR OR VITAL SIGNS M 1980-07-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2118418. Last updated year: 2026. Please use registration number 2118418 when referencing this establishment in official correspondence.
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