Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008294723

FEI Number

3008294723

Entity Name

DUMOTECH, LLC.

City/State/Country

Caledonia, MI, US

Establishment Address

6758 E Paris Ave SE, Caledonia, MI 49316, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Dumotech, LLC. (Owner Number: 10031400)

Owner / Operator Contact Address

6758 East Paris Ave. SE, Caledonia, MI 49316, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

500/0600

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KNX	Collector, Urine, (And Accessories) For Indwelling Catheter	Gastroenterology, Urology	Class 2	876.5250	2010-02-19

Official Correspondent

Duc Duong

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dumotech, LLC.

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
K791969	Medline Industries, Inc.	DYNACOR STERILE CLOSED SYS. DRAINAGE BAG	1979-11-05

Similar Registrations

Registration Number	Establishment Name	Location
1018233	C.R. BARD, INC.	COVINGTON, GA, US
3012445205	AMSINO MEDICAL GROUP (HK) COMPANY LIMITED	HONG KONG, HK
9680890	RIBBEL INTERNATIONAL LTD.	SONEPAT Haryana, IN
3006082230	C.R. BARD, INC.	MADISON, GA, US
3031582449	JM MEDICAL CO., LTD.	Liaocheng Shandong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008294723. Last updated year: 2026. Please use registration number 3008294723 when referencing this establishment in official correspondence.