GUNNELL, Inc.

FDA Device Registration & Listing · Elk City, OK, US · Registration 3009255757

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
3009255757
FEI Number
3009255757
Entity Name
GUNNELL, Inc.
City/State/Country
Elk City, OK, US
Establishment Address
321 W 12th St, Elk City, OK 73644, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Gunnell Inc. (Owner Number: 10059385)
Owner / Operator Contact Address
321 W 12th St, Elk City, OK 73644, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Gunnell Inc

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNN Components, Wheelchair Physical Medicine Class 1 890.3920 2018-12-31

Official Correspondent

Neil Bacoski

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Gunnell 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 3009255757. Last updated year: 2026. Please use registration number 3009255757 when referencing this establishment in official correspondence.
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