Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013758626

FEI Number

3013758626

Entity Name

BARAKA

City/State/Country

Santa Rosa, CA, US

Establishment Address

3451 Airway Dr. Suite G1, Santa Rosa, CA 95403, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Baraka Sinus Products (Owner Number: 10055429)

Owner / Operator Contact Address

3451 Airway Dr. Suite G1, Santa Rosa, CA 95403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Baraka Neti Pot

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCJ	Applicator, Ent	Ear, Nose, Throat	Class 1	874.5220	2017-07-24

Official Correspondent

Susan Libby

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Baraka Sinus Products

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 3013758626. Last updated year: 2026. Please use registration number 3013758626 when referencing this establishment in official correspondence.