MINNESOTA MEDTEC, INC.

FDA Device Registration & Listing · MAPLE GROVE, MN, US · Registration 2134626

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
2134626
FEI Number
3003007911
Entity Name
MINNESOTA MEDTEC, INC.
City/State/Country
MAPLE GROVE, MN, US
Establishment Address
11760 Justen Circle, Mail drop Unit B, MAPLE GROVE, MN 55369, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MINNESOTA MEDTEC, INC. (Owner Number: 9036710)
Owner / Operator Contact Address
11760 JUSTEN CIRCLE UNIT B, --, Osseo, MN 55369, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MCOMPASS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OFL Percutaneous Sheath Introducer Kit Cardiovascular Class 2 870.1340 2015-01-13
LWT Occluder, Balloon, Vena-Cava Unknown Class 3 N/A 2015-01-13
KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube Gastroenterology, Urology Class 2 876.1725 2025-08-11

Official Correspondent

BRIAN PACKARD

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MINNESOTA MEDTEC, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2134626. Last updated year: 2026. Please use registration number 2134626 when referencing this establishment in official correspondence.
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