Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3001401122

FEI Number

3001401122

Entity Name

WIELAND DESIGNS INC.

City/State/Country

Goshen, IN, US

Establishment Address

901 E Madison St, Goshen, IN 46528, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Wieland Designs Inc. (Owner Number: 10035115)

Owner / Operator Contact Address

901 East Madison, Goshen, IN 46526, 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
FML	Chair, Blood Donor	General Hospital	Class 1	880.6140	2013-08-23

Official Correspondent

Randall Bond

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Wieland Designs 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 3001401122. Last updated year: 2026. Please use registration number 3001401122 when referencing this establishment in official correspondence.