Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029923636

FEI Number

3029923636

Entity Name

ANNABELLA TECH

City/State/Country

Kfar Saba Central, IL

Establishment Address

23/5 Hataas, Kfar Saba Central 4442525, IL

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Annabella Tech (Owner Number: 10088803)

Owner / Operator Contact Address

23/5 Hataas, Kfar Saba, IL-M 4442525, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K241506

PMA Number

N/A

All Registered Proprietary Names

Annabella Double Breast Pump

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HGX	Pump, Breast, Powered	Obstetrics/Gynecology	Class 2	884.5160	2024-07-04

Official Correspondent

Dalia Dickman

US Agent Details

Stephen Lieberman Email: lieberman@donawa.com Phone: (561) 3020777

Related Public Records

Same Entity

Annabella Tech

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3031841858	Annabella Technologies Inc.	N Palm Beach, FL, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K190465	Hygeia II Medical Group, Inc.	Evolve Breast Pump	2019-10-18
K021739	Limerick, Inc.	LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002	2003-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029923636. Last updated year: 2026. Please use registration number 3029923636 when referencing this establishment in official correspondence.