LIANJIA (ZHONGSHAN) GONGMAO CO.LTD

FDA Device Registration & Listing · Zhongshan Guangdong, CN · Registration 3027517735

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
3027517735
FEI Number
3027517735
Entity Name
LIANJIA (ZHONGSHAN) GONGMAO CO.LTD
City/State/Country
Zhongshan Guangdong, CN
Establishment Address
District A, No.9 Haotou Avenue, Haotou Village, Torch Development Zone, Zhongshan City, Zhongshan Guangdong 528437, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
LIANJIA (ZHONGSHAN) GONGMAO CO.LTD (Owner Number: 10087993)
Owner / Operator Contact Address
District A, No.9 Haotou Avenue, Haotou Village, Torch Development Zone, Zhongshan City, Zhongshan, CN-GD 528437, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LIFT, PATIENT, NON-AC-POWERED SLING

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2023-05-24

Official Correspondent

Tina Huang

US Agent Details

Tony LEE Email: joyce.tsai@newprokin.com Phone: (469) 5929596

Related Public Records

Same Entity

LIANJIA (ZHONGSHAN) GONGMAO CO.LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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 3027517735. Last updated year: 2026. Please use registration number 3027517735 when referencing this establishment in official correspondence.
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