NEODEX CORP.

FDA Device Registration & Listing · Geumcheon-gu Seoul, KR · Registration 3034246182

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
3034246182
FEI Number
3034246182
Entity Name
NEODEX CORP.
City/State/Country
Geumcheon-gu Seoul, KR
Establishment Address
112, B1, 254, Beotkkot-ro, Geumcheon-gu Seoul 08511, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NeoDex Corp. (Owner Number: 10092060)
Owner / Operator Contact Address
112, B1, 254, Beotkkot-ro, Geumcheon-gu, KR-11 08511, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Hippo-D Hippo-U

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KBN Gag, Mouth Ear, Nose, Throat Class 1 874.4420 2024-11-29

Official Correspondent

Yeonwoo Lee

US Agent Details

Catherine Oh Email: catherine@cticert.co.kr Phone: (646) 2451153

Related Public Records

Same Entity

NeoDex Corp.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3034246182. Last updated year: 2026. Please use registration number 3034246182 when referencing this establishment in official correspondence.
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