HUOT INSTRUMENTS, LLC

FDA Device Registration & Listing · MENOMONEE FALLS, WI, US · Registration 3005934371

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
3005934371
FEI Number
3005934371
Entity Name
HUOT INSTRUMENTS, LLC
City/State/Country
MENOMONEE FALLS, WI, US
Establishment Address
N59 W14508 Bobolink Ave., MENOMONEE FALLS, WI 53051, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Huot Instruments, LLC (Owner Number: 9086971)
Owner / Operator Contact Address
N59W14508 Bobolink Avenue, Menomonee Falls, WI 53051, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

StarTrol

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KZF Device, Medical Examination, Ac Powered General Hospital Class 1 880.6320 2010-03-01

Official Correspondent

RICHARD WARD

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Huot Instruments, LLC
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
K851742 Burton Medical Products Corp. MEDICAL EXAMINATION LIGHTS 1985-05-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005934371. Last updated year: 2026. Please use registration number 3005934371 when referencing this establishment in official correspondence.
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