PMWCORPORATION

FDA Device Registration & Listing · Ulsan, KR · Registration 3017252880

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
3017252880
FEI Number
3017252880
Entity Name
PMWCORPORATION
City/State/Country
Ulsan, KR
Establishment Address
Room A, 2F, 135, Cheoyongsaneop 3-gil, Cheongnyang-eup, Ulju-gun, Ulsan 44988, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PMWCORPORATION (Owner Number: 10075535)
Owner / Operator Contact Address
Room A, 2F, 135, Cheoyongsaneop 3-gil, Cheongnyang-eup, Ulju-gun, Ulsan, KR-31 44988, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PARA FLOCKED SWAB GB946OP PMW Flocked Swab PMW-SWAB OP2 RADI Flocked Swab OD103NB PMW Flocked Swab PMW-NS SWAB PMW Spun Swab PMW RAYON SWAB PMW Flocked Swab PMW-SWAB DUAL PARA FLOCKED SWAB GB946NP PMW Flocked Swab PMW-SWAB NP1 SMART DIAGNOSTIC's FLOCKED SWAB SD304D SMART DIAGNOSTIC's FLOCKED SWAB SD304O PMW-SWAB PMW CONTROL SWAB PMW Spun Swab PMW POLYESTER SPUN SWAB RADI Flocked Swab OD103OB PARA POLYESTER SWAB GB946PS SMART DIAGNOSTIC's FLOCKED SWAB SD304N RADI Flocked Swab OD103DB PARA FLOCKED SWAB GB946DP PMW Spun Swab PMW RAYON SWAB PARA FLOCKED SWAB GB946NP SMART DIAGNOSTIC's FLOCKED SWAB SD304D PMW Flocked Swab PMW-NS SWAB SMART DIAGNOSTIC's FLOCKED SWAB SD304O PMW-SWAB PMW CONTROL SWAB PARA FLOCKED SWAB GB946DP SMART DIAGNOSTIC's FLOCKED SWAB SD304N RADI Flocked Swab OD103DB PMW Flocked Swab PMW-SWAB OP2 PARA FLOCKED SWAB GB946OP PMW Spun Swab PMW POLYESTER SPUN SWAB PMW Flocked Swab PMW-SWAB DUAL RADI Flocked Swab OD103OB PMW Flocked Swab PMW-SWAB NP1 RADI Flocked Swab OD103NB PARA POLYESTER SWAB GB946PS PMW-SWAB PMW CONTROL SWAB L15

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 2020-06-18
KXG Applicator, Absorbent Tipped, Sterile General Hospital Class 1 880.6025 2020-09-02

Official Correspondent

Jeong Yong Yoon

US Agent Details

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

Related Public Records

Same Entity

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017252880. Last updated year: 2026. Please use registration number 3017252880 when referencing this establishment in official correspondence.
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