FIVE STAR PLASTICS

FDA Device Registration & Listing · Eau Claire, WI, US · Registration 3007620861

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
3007620861
FEI Number
3007620861
Entity Name
FIVE STAR PLASTICS
City/State/Country
Eau Claire, WI, US
Establishment Address
1339 Continental Dr, Eau Claire, WI 54701, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Five Star Plastics (Owner Number: 10088464)
Owner / Operator Contact Address
1339 Continental Dr, Eau Claire, WI 54701, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JOJ Indicator, Physical/Chemical Sterilization Process General Hospital Class 2 880.2800 2024-11-06

Official Correspondent

Timothy DeWanz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Five Star Plastics
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2007 N/A 2
3M Comply 1248 Gas Plasma Chemical Indicator Strips for use in STERRAD 100, STERRAD 100S and STERRAD 50 Sterilization Systems. Indicator for hydrogen peroxide sterilant.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007620861. Last updated year: 2026. Please use registration number 3007620861 when referencing this establishment in official correspondence.
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