PLASTI-PRODUCTS, INC.

FDA Device Registration & Listing · OMAHA, NE, US · Registration 1930034

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
1930034
FEI Number
1930034
Entity Name
PLASTI-PRODUCTS, INC.
City/State/Country
OMAHA, NE, US
Establishment Address
9904 N 109th Ave, OMAHA, NE 68142, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PLASTI-PRODUCTS, INC. (Owner Number: 1930034)
Owner / Operator Contact Address
9904 N109th Ave, Omaha, NE 68142, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K970383
PMA Number
N/A

All Registered Proprietary Names

Monoject Horizontal Entry Sharps Container PLASTI PAN GRAD URI PAN PAN II VERTICAL HORZONTAL ENTRY SHARPS CONTAINER Plasti Grad VERTICAL HORZONTAL ENTRY SHARPS CONTAINER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2026-06-16
FOB Bedpan General Hospital Class 1 880.6730 2001-08-08
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2006-03-30
NNI Container, Specimen, Non-Sterile Pathology Class 1 864.3250 2012-12-28
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2006-03-30

Official Correspondent

DANIEL BROWN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PLASTI-PRODUCTS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1930034. Last updated year: 2026. Please use registration number 1930034 when referencing this establishment in official correspondence.
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