Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042903214

FEI Number

3042903214

Entity Name

KUSMO

City/State/Country

Chico, CA, US

Establishment Address

1645 Esplanade Ste 3, Chico, CA 95926, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Kusmo (Owner Number: 10094612)

Owner / Operator Contact Address

1645 Esplanade suite #3, Chico, CA 95928, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CaTHSTiX

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMK	Device, Intravascular Catheter Securement	General Hospital	Class 1	880.5210	2025-12-10

Official Correspondent

Walter kusumoto

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kusmo

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3030433705	TMR PLASTICS	Bydgoszcz Pomorskie, PL
8030607	Industrias Apson S.A de C.V	AGUA PRIETA Sonora, MX
3011642792	Merit Maquiladora Mexico, S. DE R.L. DE C.V.	Tijuana Baja California, MX
3005023997	Shanghai Chuangshi Medical Technology (Group) Co., Ltd.	SHANGHAI, CN
3003152976	BECTON DICKINSON, S.A.	SAN AGUSTIN DE GUADALIX Madrid (Province), ES

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042903214. Last updated year: 2026. Please use registration number 3042903214 when referencing this establishment in official correspondence.