Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033520596

FEI Number

3033520596

Entity Name

INOT CO., LTD.

City/State/Country

Uiwang Gyeonggi, KR

Establishment Address

(Indukwon IT Valley, Foil-dong) 504, 505 B-dong, 40, Imiro, Uiwang Gyeonggi 16006, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

INOT CO., Ltd. (Owner Number: 10091742)

Owner / Operator Contact Address

(Indukwon IT Valley, Foil-dong) 504, 505 B-dong, 40, Imiro, Uiwang, KR-41 16006, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SILICONE STRIP ACRYL STRIP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KGS	Retention Device, Suture	General, Plastic Surgery	Class 1	878.4930	2025-11-19

Official Correspondent

Sung Chul Hur

US Agent Details

Joyce Kwon Business: PROVISION CONSULTING GROUP, INC. Email: ask@provisionfda.com Phone: (909) 4933276

Related Public Records

Same Entity

INOT 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 3033520596. Last updated year: 2026. Please use registration number 3033520596 when referencing this establishment in official correspondence.