Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1933015

FEI Number

1000218822

Entity Name

INTEGRITY PRODUCTS, INC.

City/State/Country

Grandview, MO, US

Establishment Address

4006 Main St., Grandview, MO 64030, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Integrity Products, Inc. (Owner Number: 10054763)

Owner / Operator Contact Address

4006 Main St., Grandview, MO 64030, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Integrity Cup Specimen Cup Leakbuster

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2017-04-24
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2021-03-08

Official Correspondent

Jeff Bailey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Integrity Products, 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 1933015. Last updated year: 2026. Please use registration number 1933015 when referencing this establishment in official correspondence.