UNIMOM CO.

FDA Device Registration & Listing · Osan-si Gyeonggi, KR · Registration 3012298445

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
3012298445
FEI Number
3012298445
Entity Name
UNIMOM CO.
City/State/Country
Osan-si Gyeonggi, KR
Establishment Address
110-19, GAJANGSANEOPSEOBUK-RO, Osan-si Gyeonggi 18102, KR
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Unimom Co. (Owner Number: 10053086)
Owner / Operator Contact Address
110-19, Gajangsaneopseobuk-ro, Osan-si, KR-41 18102, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Opera eco Opera Unimom Nipple (NIPPLE, FEEDER)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PWA Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure Obstetrics/Gynecology Class 1 884.5150 2018-12-12
HGX Pump, Breast, Powered Obstetrics/Gynecology Class 2 884.5160 2019-09-23
HFS Shield, Nipple General Hospital Class 1 880.5630 2018-01-25
FNN Nipple, Lambs Feeding General Hospital Class 1 880.5640 2018-02-01

Official Correspondent

Sang Hyun Hong

US Agent Details

Jung Ryun Ahn Business: KMC USA, Inc Email: kmc.usa@kmcerti.com Phone: (646) 3576058

Related Public Records

Same Entity

Unimom Co.
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 3012298445. Last updated year: 2026. Please use registration number 3012298445 when referencing this establishment in official correspondence.
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