STEELCASE INC.

FDA Device Registration & Listing · Grand Rapids, MI, US · Registration 3000122531

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
3000122531
FEI Number
3000122531
Entity Name
STEELCASE INC.
City/State/Country
Grand Rapids, MI, US
Establishment Address
901 44TH ST SE, Grand Rapids, MI 49508, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Steelcase Inc (Owner Number: 10045456)
Owner / Operator Contact Address
901, 44 th Street SE, Grand Rapids, MI 49508, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mitra recliners Empath recliners Mineral recliners

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRK Chair, Examination And Treatment General Hospital Class 1 880.6140 2013-11-19

Official Correspondent

Caryn Stetson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Steelcase Inc
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 3000122531. Last updated year: 2026. Please use registration number 3000122531 when referencing this establishment in official correspondence.
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