Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012956357

FEI Number

3012956357

Entity Name

IISM INC.

City/State/Country

Sejong-si, KR

Establishment Address

Room 402, 7-16, Naseongnam-ro, Sejong-si, Sejong-si 30129, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

iiSM Inc. (Owner Number: 10050615)

Owner / Operator Contact Address

Room 402, 7-16, Naseongnam-ro, Sejong-si, Sejong-si, KR-50 30129, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VPism-A VPism-C+ VPism-D+

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KZA	Device, Vein Location, Liquid Crystal	General Hospital	Class 1	880.6970	2015-12-08

Official Correspondent

Younjin Kim

US Agent Details

MINSEOB JO Email: msjoe@gst-in.com Phone: (737) 2055448

Related Public Records

Same Entity

iiSM Inc.

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 3012956357. Last updated year: 2026. Please use registration number 3012956357 when referencing this establishment in official correspondence.