Virtex

FDA Device Registration & Listing · ANOKA, MN, US · Registration 2183673

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
2183673
FEI Number
2183673
Entity Name
Virtex
City/State/Country
ANOKA, MN, US
Establishment Address
6700 Bunker Lake Blvd. NW, ANOKA, MN 55303, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Virtex (Owner Number: 2183673)
Owner / Operator Contact Address
6700 BUNKER LAKE BLVD., --, Anoka, MN 55303, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

199235- 199235

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNT Tubes, Gastrointestinal (And Accessories) Gastroenterology, Urology Class 2 876.5980 2008-03-28
LIL Monitor, Penile Tumescence Unknown Class U N/A 2020-12-18
LZH Pump, Infusion, Enteral General Hospital Class 2 880.5725 2008-04-02

Official Correspondent

Doreen Douvier

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Virtex
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
K900590 Biosearch Medical Products, Inc. BIOSEARCH DOBBHOFF(R) GASTROTRAC JEJUNAL FEEDING 1990-08-02
K102548 Footprint Medical, Inc. FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE 2010-11-26
K955248 United States Endoscopy Group, Inc. U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT 1996-05-21
K872921 Medical Support, Inc. MSS ENTERAL DELIVERY SET 1987-12-03
K180622 Covidien Kangaroo Gastrostomy Feeding Tube with ENFit Y-Port 2018-10-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183673. Last updated year: 2026. Please use registration number 2183673 when referencing this establishment in official correspondence.
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