Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3001632652

FEI Number

3001632652

Entity Name

BUDNICK CONVERTING, INC.

City/State/Country

Columbia, IL, US

Establishment Address

340 Parkway Drive, Columbia, IL 62236, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Budnick Converting, Inc. (Owner Number: 10056541)

Owner / Operator Contact Address

340 Parkway Dr, Columbia, IL 62236, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ABSORBER, SALIVA, PAPER

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KHR	Absorber, Saliva, Paper	Dental	Class 1	872.6050	2017-12-20

Official Correspondent

Allison Ferry

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Budnick Converting, Inc.

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 3001632652. Last updated year: 2026. Please use registration number 3001632652 when referencing this establishment in official correspondence.