Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3001122163

FEI Number

3001122163

Entity Name

KENT MANUFACTURING COMPANY

City/State/Country

Grand Rapids, MI, US

Establishment Address

2200 OAK INDUSTRIAL DR NE, Grand Rapids, MI 49505, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Kent Manufacturing Company (Owner Number: 10054913)

Owner / Operator Contact Address

2200 Oak Industrial Dr, Grand Rapids, MI 49505, US

Initial Importer Flag

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
EGD	Wax, Dental, Intraoral	Dental	Class 1	872.6890	2017-05-11

Official Correspondent

Steve Denhof

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kent Manufacturing Company

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001122163. Last updated year: 2026. Please use registration number 3001122163 when referencing this establishment in official correspondence.