HUMANE RESTRAINT CO., INC.

FDA Device Registration & Listing · Middleton, WI, US · Registration 2126660

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
2126660
FEI Number
2126660
Entity Name
HUMANE RESTRAINT CO., INC.
City/State/Country
Middleton, WI, US
Establishment Address
912 BETHEL CIR, Middleton, WI 53597, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HUMANE RESTRAINT, INC. (Owner Number: 9921003)
Owner / Operator Contact Address
912 BETHEL CIRCLE, --, Waunakee, WI 53597, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Humane Restraint NYLON AND COTTON BELTS NYLON AND COTTON BOLTS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMQ Restraint, Protective General Hospital Class 1 880.6760 2021-11-11
IQB Belt, Wheelchair Physical Medicine Class 1 890.3920 1992-06-18

Official Correspondent

STACY SCHULTZ

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HUMANE RESTRAINT, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K962327 Sekure Seat Corp. SEKURE SEAT ADULT PASSIVE RESTRAINING DEVICE 1997-03-06
K963243 Heelbo, Inc. HEELBO BLAZER SLEEVED JACKET 1996-10-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2126660. Last updated year: 2026. Please use registration number 2126660 when referencing this establishment in official correspondence.
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