CHIYEWON CO., LTD.

FDA Device Registration & Listing · Guri-si Gyeonggi, KR · Registration 3011802717

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
3011802717
FEI Number
3011802717
Entity Name
CHIYEWON CO., LTD.
City/State/Country
Guri-si Gyeonggi, KR
Establishment Address
1F, 3F, 196, Donggureung-ro,, Guri-si Gyeonggi 11909, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Chiyewon Co., Ltd. (Owner Number: 10049595)
Owner / Operator Contact Address
1F, 3F, 196, Donggureung-ro, Guri-si, KR-41 11909, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NPM Bone Grafting Material, Animal Source Dental Class 2 872.3930 2015-06-25

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Chiyewon Co., Ltd.
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 3011802717. Last updated year: 2026. Please use registration number 3011802717 when referencing this establishment in official correspondence.
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