INDUSTRIAL WOODWORKING CORP.

FDA Device Registration & Listing · Zeeland, MI, US · Registration 3003904216

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
3003904216
FEI Number
3003904216
Entity Name
INDUSTRIAL WOODWORKING CORP.
City/State/Country
Zeeland, MI, US
Establishment Address
9380 Pentatech Dr., Zeeland, MI 49464, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Industrial Woodworking Corp. (Owner Number: 10024548)
Owner / Operator Contact Address
9380 Pentatech Dr., PO Box 286, Zeeland, MI 49464, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MedViron Guardian Bassinet Bassinet-Shaker Bassinett-Modern Bassinet-Euro Bassinet-Traditional MedViron Guardian Rise Bassinet MedViron Guardian Rise II Bassinet

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NZG Bassinet, Hospital General Hospital Class 2 880.5145 2008-02-13

Official Correspondent

Bradford Davis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Industrial Woodworking Corp.
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 3003904216. Last updated year: 2026. Please use registration number 3003904216 when referencing this establishment in official correspondence.
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