NEOMEDI PHARM INC.

FDA Device Registration & Listing · GOYANG-SI Gyeonggi, KR · Registration 3013115058

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
3013115058
FEI Number
3013115058
Entity Name
NEOMEDI PHARM INC.
City/State/Country
GOYANG-SI Gyeonggi, KR
Establishment Address
301, 3F, 142, ILSAN-RO, ILSANGONG-GU, GOYANG-SI Gyeonggi 10442, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NEOMEDI PHARM Inc. (Owner Number: 10079747)
Owner / Operator Contact Address
301, 3F, 142, ILSAN-RO, ILSANGONG-GU, GOYANG-SI, KR-41 10442, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MOMSDERM NEO AQUA DRESSING MOMSDERM EURO NEO Aqua Bandage MOMSDERM NEO Aqua Dressing MOMSDERM HYDROCOLLOID BAND MOMSDERM A NEO Dressing MOMSDERM NEO DRESSING MOMSDERM AQUA BAND SKIN CARE PLUS NEO SOFTFOAM Skin Care Plus alpha Momsderm Non Woven Retention Tape NEO BAND PLUS NEO LIFE MASK (KF-AD) NEO LIFE MASK (KF-94)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2020-12-21
QKR Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua Unknown Class N N/A 2020-12-21

Official Correspondent

SANG MIN LEE

US Agent Details

chuljoo jeon Business: KTR Americas Inc. Email: americas@ktr.or.kr Phone: (562) 3172865

Related Public Records

Same Entity

NEOMEDI PHARM Inc.
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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013115058. Last updated year: 2026. Please use registration number 3013115058 when referencing this establishment in official correspondence.
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