MIDWAY MEDICAL

FDA Device Registration & Listing · Bloomington, IL, US · Registration 3015536408

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
3015536408
FEI Number
3015536408
Entity Name
MIDWAY MEDICAL
City/State/Country
Bloomington, IL, US
Establishment Address
3004 Gill Street, Building 100, Bloomington, IL 61704, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Midway Medical (Owner Number: 10061377)
Owner / Operator Contact Address
3004 Gill Street, Building 100, Bloomington, IL 61704, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K190975
PMA Number
N/A

All Registered Proprietary Names

Plexus Portable DVT Therapy System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOW Sleeve, Limb, Compressible Cardiovascular Class 2 870.5800 2019-10-15

Official Correspondent

Eric Rohde

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Midway Medical
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
K170216 Tactile Systems Technology, Inc. (Dba Tactile Medical) Flexitouch System 2017-05-26
K100306 Covidien KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES 2010-05-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015536408. Last updated year: 2026. Please use registration number 3015536408 when referencing this establishment in official correspondence.
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