AMERICAN PLASTICS CO., INC.

FDA Device Registration & Listing · Glendale, AZ, US · Registration 3043513097

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3043513097
FEI Number
3043513097
Entity Name
AMERICAN PLASTICS CO., INC.
City/State/Country
Glendale, AZ, US
Establishment Address
6821 N 55th Ave, Glendale, AZ 85301, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
American Plastics Co., Inc. (Owner Number: 10095009)
Owner / Operator Contact Address
6821 N 55th Ave, Glendale, AZ 85301, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Urine Tube

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MPQ Container, Specimen, Urine, Drugs Of Abuse, Over The Counter Pathology Class 1 864.3260 2026-01-14

Official Correspondent

Leslie Steinberg

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

American Plastics Co., Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043513097. Last updated year: 2026. Please use registration number 3043513097 when referencing this establishment in official correspondence.
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