NURIMEDICS CO., LTD

FDA Device Registration & Listing · Gimpo-si Gyeonggi, KR · Registration 3017930281

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
3017930281
FEI Number
3017930281
Entity Name
NURIMEDICS CO., LTD
City/State/Country
Gimpo-si Gyeonggi, KR
Establishment Address
11, Hasa-ro, Haseong-myeon, Gimpo-si Gyeonggi 10013, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NURIMEDICS CO., LTD (Owner Number: 10086367)
Owner / Operator Contact Address
11, Hasa-ro, Haseong-myeon, Gimpo-si, KR-41 10013, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MADECA MEDI PATCH FREE-CUT PATCH DERMADOT INVISIBLE PIMPLE PATCHES EVERYDAY SPOT CONTROL EMERGENCY SPOT TREATMENT MADECA MEDI PATCH AC Q Hydrocolloid Dressing MADECA MEDI PATCH SPECIAL COLOR MADECA MEDI PATCH SPOT PATCH Madeca Summer Aroma Patch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic General, Plastic Surgery Class 1 878.4022 2022-11-03
NAD Dressing, Wound, Occlusive General, Plastic Surgery Class 1 878.4020 2024-08-13
IMC Bath, Paraffin Physical Medicine Class 2 890.5110 2026-01-20

Official Correspondent

No official correspondent registered.

US Agent Details

Grace Kim Business: JS INTERNATIONAL HOLDING Email: ahn3060@naver.com Phone: (310) 5983012

Related Public Records

Same Entity

NURIMEDICS CO., LTD
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
K881936 Iberhospitex, S.A. OPER-FILM-ADHESIVE MEMBRANE 1988-08-31

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2019 COVIDIEN LLC 1
Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the dressing.
Z-0014-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100% Cotton, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m), REF 6715 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0015-2019 COVIDIEN LLC 1
Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0016-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0017-2019 COVIDIEN LLC 1
Dermacea Gauze Fluff Roll, 6 Ply, 4-1/2 x 4-1/8 yd (11.4 cm x 3.7 m), REF 441103 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

Similar Registrations

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3043012215 ZENESIS HOLDINGS CO., LIMITED Kowloon, HK
3008646686 KIKGEL Ujazd Opolskie, PL
8043484 Smith & Nephew Medical Ltd HULL East Riding of Yorkshire, GB
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017930281. Last updated year: 2026. Please use registration number 3017930281 when referencing this establishment in official correspondence.
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