KAR BOW INDUSTRIES CO., LTD.

FDA Device Registration & Listing · Dongguan Guangdong, CN · Registration 3012436530

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
3012436530
FEI Number
3012436530
Entity Name
KAR BOW INDUSTRIES CO., LTD.
City/State/Country
Dongguan Guangdong, CN
Establishment Address
No. 41, Jiatang Lane, Hanxishui Village, Chashan Town, Dongguan Guangdong 528400, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Kar Bow Industries Co., Ltd. (Owner Number: 10050262)
Owner / Operator Contact Address
No. 41, Jiatang Lane, Hanxishui Village, Chashan Town, Dongguan City, CN-GD 523000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

#KB-1696 #KB-1697 #13408 #KB-1698 #13405 #3060 Fluorescent Eye Cabinet Lamp Trumpet pole + Gooseneck Floor Lamps

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KZF Device, Medical Examination, Ac Powered General Hospital Class 1 880.6320 2015-10-26

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

Kar Bow Industries 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
K851742 Burton Medical Products Corp. MEDICAL EXAMINATION LIGHTS 1985-05-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012436530. Last updated year: 2026. Please use registration number 3012436530 when referencing this establishment in official correspondence.
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