INERTIA INC.

FDA Device Registration & Listing · Daejeon,, KR · Registration 3023278903

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
3023278903
FEI Number
3023278903
Entity Name
INERTIA INC.
City/State/Country
Daejeon,, KR
Establishment Address
193, Munji-ro, Yuseong-gu, Daejeon, 34051, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
INERTIA Inc. (Owner Number: 10085566)
Owner / Operator Contact Address
193, Munji-ro, Yuseong-gu, Daejeon,, KR-30 34051, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Inertia Organic Cotton Cover Period Underwear The Prism (X-Large) Inertia organic cotton pads the prism (large) Inertia organic cotton pads the prism (regular) Inertia Organic Cotton Cover Period Underwear The Prism (Large) Inertia the prism organic cotton cover Daily Liners Inertia Organic Cotton Cover Period Underwear The Prism (Regular) Inertia organic cotton cover pads the perfection (regular) Inertia organic cotton cover pads the perfection (large)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2022-07-03

Official Correspondent

Hyoyi Kim

US Agent Details

Eddie Young Business: American Technology Clinical Solutions, Inc. Email: atcs4004@gmail.com Phone: (916) 9408899

Related Public Records

Same Entity

INERTIA Inc.
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
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023278903. Last updated year: 2026. Please use registration number 3023278903 when referencing this establishment in official correspondence.
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