LIGHTS MEDICAL MANUFACTURE CO., LTD.

FDA Device Registration & Listing · TIANJIN CITY, TIANJIN, CN · Registration 3004472810

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
3004472810
FEI Number
3005310494
Entity Name
LIGHTS MEDICAL MANUFACTURE CO., LTD.
City/State/Country
TIANJIN CITY, TIANJIN, CN
Establishment Address
NO. 19, QUANDA ROAD, WUQING DEVELOPMENT AREA, TIANJIN CITY, TIANJIN 301700, CN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
LIGHTS MEDICAL SUPPLY CO., LTD. (Owner Number: 9061455)
Owner / Operator Contact Address
NO. 19, QUANDA ROAD, WUQING DEVELOPMENT AREA, TIANJIN CITY, TIANJIN, CN-NOTA 301700, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Adhesive remove tape Alcohol Pad Lubricant

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KOX Solvent, Adhesive Tape General, Plastic Surgery Class 1 878.4730 2006-02-01
LKB Pad, Alcohol, Device Disinfectant Unknown Class U N/A 2025-12-15
KMJ Lubricant, Patient General Hospital Class 1 880.6375 2021-06-21

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Shen Business: Manton Business and Technology Services Email: cyshen@aol.com Phone: (608) 2179358

Related Public Records

Same Entity

LIGHTS MEDICAL SUPPLY CO., LTD.
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
K820587 Abco Dealers, Inc. WET PACK LINE OF PRODUCTS 1982-03-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004472810. Last updated year: 2026. Please use registration number 3004472810 when referencing this establishment in official correspondence.
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