F&M PLASTICS, INC.

FDA Device Registration & Listing · Osceola, WI, US · Registration 3005911383

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
3005911383
FEI Number
3005911383
Entity Name
F&M PLASTICS, INC.
City/State/Country
Osceola, WI, US
Establishment Address
503 Simmon Drive, Osceola, WI 54020, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
F&M Plastics (Owner Number: 10060677)
Owner / Operator Contact Address
503 Simmon Drive, Osceola, WI 54020, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Steris

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GDJ Clamp, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2019-06-20

Official Correspondent

Jeff Krenz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

F&M Plastics
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 3005911383. Last updated year: 2026. Please use registration number 3005911383 when referencing this establishment in official correspondence.
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