MILKMATE

FDA Device Registration & Listing · New York, NY, US · Registration 3027115730

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
3027115730
FEI Number
3027115730
Entity Name
MILKMATE
City/State/Country
New York, NY, US
Establishment Address
521 5th Ave Fl 18 Ste 1808, New York, NY 10175, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
MilkMate (Owner Number: 10087772)
Owner / Operator Contact Address
780 3rd Avenue, Floor 26, New York, NY 10017, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

MilkMate Insert MilkMate Breast Pump

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HFS Shield, Nipple General Hospital Class 1 880.5630 2024-02-01
HGX Pump, Breast, Powered Obstetrics/Gynecology Class 2 884.5160 2023-04-06

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MilkMate
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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 3027115730. Last updated year: 2026. Please use registration number 3027115730 when referencing this establishment in official correspondence.
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