IDION MEDICAL CO.,LTD

FDA Device Registration & Listing · Huzhou Zhejiang, CN · Registration 3008770712

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
3008770712
FEI Number
3008770712
Entity Name
IDION MEDICAL CO.,LTD
City/State/Country
Huzhou Zhejiang, CN
Establishment Address
No.519 QUYUAN NORTH ROAD,WUKANG TOWN,, DEQING,HUZHOU,ZHEJIANG PROVINCE,P.R.CHINA, Huzhou Zhejiang 313200, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
IDION MEDICAL CO.,LTD (Owner Number: 10057121)
Owner / Operator Contact Address
No.519 QUYUAN NORTH ROAD,WUKANG TOWN,, DEQING,HUZHOU,ZHEJIANG PROVINCE,P.R.CHINA, Huzhou, CN-ZJ 313200, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pulp basins Medicine cup

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FNY Basin, Emesis General Hospital Class 1 880.6730 2024-12-27
KYW Container, Liquid Medication, Graduated General Hospital Class 1 880.6430 2018-02-25

Official Correspondent

Lily Yao

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

IDION MEDICAL 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 3008770712. Last updated year: 2026. Please use registration number 3008770712 when referencing this establishment in official correspondence.
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