Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3000224270

FEI Number

3000224270

Entity Name

UNDERWOOD MOLD CO

City/State/Country

Woodstock, GA, US

Establishment Address

104 Dixie Dr, Woodstock, GA 30189, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Underwood Mold Co (Owner Number: 10094880)

Owner / Operator Contact Address

104 Dixie Drive, Woodstock, GA 30189, US

Initial Importer Flag

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
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2025-12-31

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Underwood Mold Co

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 3000224270. Last updated year: 2026. Please use registration number 3000224270 when referencing this establishment in official correspondence.