Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009474606

FEI Number

3009474606

Entity Name

AMPAC HOLDINGS, LLC

City/State/Country

Cincinnati, OH, US

Establishment Address

12025 TRICON RD, Cincinnati, OH 45246, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Proampac (Owner Number: 10045623)

Owner / Operator Contact Address

12025 Tricon Rd., Cincinnati, OH 45246, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Kapak

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2013-12-09

Official Correspondent

Clint Hatton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Proampac

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 3009474606. Last updated year: 2026. Please use registration number 3009474606 when referencing this establishment in official correspondence.