SAUDER MANUFACTURING CO

FDA Device Registration & Listing · New Haven, IN, US · Registration 3013985833

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
3013985833
FEI Number
3013985833
Entity Name
SAUDER MANUFACTURING CO
City/State/Country
New Haven, IN, US
Establishment Address
10578 Rose Avenue, New Haven, IN 46774, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Sauder Manufacturing Co (Owner Number: 10055867)
Owner / Operator Contact Address
930 West Barre Road, Archbold, OH 43502, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Versant Recliner Accord Recliner Arris Recliner Cove Recliner Capital Recliner Accord Amari

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
INN Chair, Adjustable, Mechanical Physical Medicine Class 1 890.3100 2017-10-13

Official Correspondent

Emidio Rapone

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sauder Manufacturing Co
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 3013985833. Last updated year: 2026. Please use registration number 3013985833 when referencing this establishment in official correspondence.
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