JIANGMEN K.K.PLASTIC FACTORY LTD.

FDA Device Registration & Listing · Jiangmen Guangdong, CN · Registration 3013513780

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
3013513780
FEI Number
3013513780
Entity Name
JIANGMEN K.K.PLASTIC FACTORY LTD.
City/State/Country
Jiangmen Guangdong, CN
Establishment Address
NO.193, 3rd Street Jian She RD, Jiangmen Guangdong 529000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Jiangmen K.K.Plastic Factory LTD. (Owner Number: 10053329)
Owner / Operator Contact Address
NO.193, 3rd Street Jian She RD, Jiangmen, CN-GD 529000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Liquid Medication Dispenser

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2016-11-22

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

Jiangmen K.K.Plastic Factory 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 3013513780. Last updated year: 2026. Please use registration number 3013513780 when referencing this establishment in official correspondence.
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