Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1922337

FEI Number

1922337

Entity Name

Fuller Industries, INC

City/State/Country

Great Bend, KS, US

Establishment Address

One Fuller Way, Great Bend, KS 67530, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Fuller Industries, INC (Owner Number: 10042742)

Owner / Operator Contact Address

One Fuller Way, Great Bend, KS 67530, 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
KOX	Solvent, Adhesive Tape	General, Plastic Surgery	Class 1	878.4730	2013-03-29

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Fuller Industries, INC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
1811212	FERNDALE LABORATORIES, INC.	Ferndale, MI, US
3012910884	WALTERS HOUGHTON LTD.	Sandycroft, Deeside Flintshire, GB
3006789548	VALLEY PACKAGING INDUSTRIES, INC.	Appleton, WI, US
3012494290	SANICURE BV	SCHIPHOL Noord-Holland, NL
3042024535	PT YOUMI MEDIKA INDUSTRI	Batang Sulawesi Utara, ID

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1922337. Last updated year: 2026. Please use registration number 1922337 when referencing this establishment in official correspondence.