PSI PLUS CO., LTD.

FDA Device Registration & Listing · Suwon-si Gyeonggi, KR · Registration 3023314720

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
3023314720
FEI Number
3023314720
Entity Name
PSI PLUS CO., LTD.
City/State/Country
Suwon-si Gyeonggi, KR
Establishment Address
101-404, 407, 408, 88, Sinwon-ro, Yeongtong-gu, Suwon-si Gyeonggi 16681, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PSI Plus Co., Ltd. (Owner Number: 10092365)
Owner / Operator Contact Address
101-404, 407, 408, 88, Sinwon-ro, Yeongtong-gu, Suwon-si, KR-41 16681, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mark-Vu 3D Meta-Vu

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FTT Camera, Still, Surgical General, Plastic Surgery Class 1 878.4160 2024-12-29

Official Correspondent

Dong Geon Lee

US Agent Details

PRISCILLA CHUNG Business: LK Consulting Group USA, Inc. Email: juhee.c@lkconsultinggroup.com Phone: (714) 9225276

Related Public Records

Same Entity

PSI Plus Co., Ltd.
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 3023314720. Last updated year: 2026. Please use registration number 3023314720 when referencing this establishment in official correspondence.
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