Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043842098

FEI Number

3043842098

Entity Name

Huma-Tek DeKalb Avenue

City/State/Country

Sycamore, IL, US

Establishment Address

1430 Dekalb Ave, Sycamore, IL 60178, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Huma-Tek, LLC (Owner Number: 10095361)

Owner / Operator Contact Address

1430 DeKalb Avenue, Sycamore, IL 60178, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Huma-Clamp

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FHA	Clamp, Penile	Gastroenterology, Urology	Class 1	876.5160	2026-03-03

Official Correspondent

Jamie Buckmeier

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Huma-Tek, LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3010875172	COMMUNITY MEDICAL PRODUCTS LLC	Prairie du Sac, WI, US
8040278	Falcon Surgical Co. (Pvt.) Ltd.	Sialkot Punjab, PK
3011137372	Teleflex Medical LLC	Morrisville, NC, US
9610612	AESCULAP AG	TUTTLINGEN, DONAU Baden-Wurttemberg, DE
1018233	C.R. BARD, INC.	COVINGTON, GA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043842098. Last updated year: 2026. Please use registration number 3043842098 when referencing this establishment in official correspondence.