TacPro, LLC dba Creganna Medical

FDA Device Registration & Listing · Plymouth, MN, US · Registration 2183982

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
2183982
FEI Number
1000116168
Entity Name
TacPro, LLC dba Creganna Medical
City/State/Country
Plymouth, MN, US
Establishment Address
5905 Trenton Ln N, Plymouth, MN 55442, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
TacPro,LLC dba Creganna Medical (Owner Number: 9055649)
Owner / Operator Contact Address
5905 Trenton Lane N, Plymouth, MN 55442, 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
MJN Catheter, Intravascular Occluding, Temporary Cardiovascular Class 2 870.4450 2013-01-30

Official Correspondent

Tafzeelur Rahaman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TacPro,LLC dba Creganna 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
K051067 LeMaitre Vascular, Inc. PRUITT F3 OUTLYING AND INLYING CAROTID SHUNT (WITH AND WITHOUT T-PORT) 2005-05-27
K093847 Thermopeutix, Inc. DUFLO CATHETER (HEPARIN COATED) 2010-08-25

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2009 Edwards Lifesciences, LLC 2
Edwards Lifesciences***Fogarty Fortis***Arterial Embolectomy Catheter Is indicated for the removal of fresh, soft emboli and thrombi from the vessels in the arterial system.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183982. Last updated year: 2026. Please use registration number 2183982 when referencing this establishment in official correspondence.
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