Zengcheng Hua Chang Plastic & Metal Moulding Company Limited

FDA Device Registration & Listing · Zengcheng Guangdong, CN · Registration 3008685522

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
3008685522
FEI Number
3008685522
Entity Name
Zengcheng Hua Chang Plastic & Metal Moulding Company Limited
City/State/Country
Zengcheng Guangdong, CN
Establishment Address
North Guangming Road, Zengcheng Economic, Technology Development Zone, Zengcheng Guangdong NONE, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Zengcheng Hua Chang Plastic & Metal Moulding Company Limited (Owner Number: 10042136)
Owner / Operator Contact Address
Room 1701, Wang Fai Industrial Building, 29 Luk Hop Street, San Po Kong, Kowloon, Hong Kong, HK-NOTA NONE, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Brevetti stocking and sock aid Fork Queens handle Savanah bath board Savanah Bath Step Savanah Splash Guard Savanah bath seat Sonaris

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILG Stocking, Elastic Physical Medicine Class 1 890.3475 2012-11-14
ILC Utensil, Eating Physical Medicine Class 1 890.5050 2012-11-14
ILS Adaptor, Hygiene Physical Medicine Class 1 890.5050 2012-11-14
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2012-10-23

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

Zengcheng Hua Chang Plastic & Metal Moulding Company Limited
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
K830425 Maddak, Inc. TOILET SEAT RAISED 1983-05-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2018 Handicare Usa Inc 1
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018 Handicare AB Maskinvagen 1
Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008685522. Last updated year: 2026. Please use registration number 3008685522 when referencing this establishment in official correspondence.
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