Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2183585

FEI Number

2183585

Entity Name

Dujo Logos Inc. DBA: MEDICOMP MEDICAL

City/State/Country

Princeton, MN, US

Establishment Address

12535 316TH AVE NW, Princeton, MN 55371, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

MEDICOMP (Owner Number: 2183585)

Owner / Operator Contact Address

12535 316TH AVE NW, PO Box 322, Princeton, MN 55371, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MEDICOMP MANUAL PERCUSSOR CUP MEDICOMP ADULT BACTERIA/VIRAL FILTER MEDICOMP CONNECTOR, AIRWAY (EXTENSION) MEDICOMP HEAT MOISTURE EXCHANGER

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GWZ	Percussor	Neurology	Class 1	882.1700	2008-12-04
CAH	Filter, Bacterial, Breathing-Circuit	Anesthesiology	Class 2	868.5260	2007-11-16
BZA	Connector, Airway (Extension)	Anesthesiology	Class 1	868.5810	2008-12-04
BYD	Condenser, Heat And Moisture (Artificial Nose)	Anesthesiology	Class 1	868.5375	2003-04-29

Official Correspondent

DUNCAN JOHNSON

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MEDICOMP

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
K962045	Mallinckrodt Medical	ANESTHESIA BREATHING CIRCUIT/ANESTHESIA BREATHING KIT	1996-11-26

Similar Registrations

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9710524	ULTIMATE MEDICAL PRODUCTS LTD.	SHARJAH Ash Shariqah, AE
3003418325	Integra LifeSciences Corporation	Princeton, NJ, US
9611283	DIMEDA INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE
3035708926	MED2B LTD.	Kitzingen Bavaria, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183585. Last updated year: 2026. Please use registration number 2183585 when referencing this establishment in official correspondence.