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Data / Medical devices / China / Guangzhou Baoli Hardware & Electronic Co.,ltd.

Guangzhou Baoli Hardware & Electronic Co.,ltd.: FDA-registered device maker in Guangzhou Guangdong, China, 1 510(k) clearance

Guangzhou Baoli Hardware & Electronic Co.,ltd. is registered with the FDA (registration 3013823570) in Guangzhou Guangdong, China. It lists 20 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 10, 2011. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3013823570
Address
Zhongyi Industrial Park,Zhongcun Town,Panyu Dristrict, Guangzhou Guangdong, China, 511495
Owner or operator
Guangzhou Baoli Hardware & Electronic CO.,LTD. (10060897)
Roles
Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler
First device listed
July 9, 2019
Registered through
2026
Brand names listed
Adult Bedrail AR03, AR04, AR05, AR07, Comfortable Protective Mask, Disposable Face Mask, Disposable Isolation Garment, Disposable hat, Disposable protective foot cover, Elbow crutch AH05, Face shield and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Adaptor, HygieneILS1Exporter to the US, Manufactureraccessdata.fda.gov
Adaptor, RecreationalILT1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Adult Portable Bed Rails For Medical PurposesQTC1Exporter to the US, Manufactureraccessdata.fda.gov
Aid, TransferIKX1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Bed, ManualFNJ1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Cane, Safety WalkKHY1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Cap, SurgicalFYF1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Continuous Measurement ThermometerFLL2Exporter to the US, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Cover, Mattress (Medical Purposes)FMW1Exporter to the US, Manufactureraccessdata.fda.gov
Cover, Shoe, Operating-RoomFXP1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Disinfectant, Medical DevicesLRJ1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Dispenser, Liquid MedicationKYX1Exporter to the US, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Dropper, EntKCM1Exporter to the US, Manufactureraccessdata.fda.gov
Non-Surgical GownOEA1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Pad, Alcohol, Device DisinfectantLKBUExporter to the US, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Respirator, SurgicalMSH2Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)HOY1Exporter to the US, Manufactureraccessdata.fda.gov
Syringe, Irrigating (Non Dental)KYZ1Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Toothbrush, ManualEFW1Exporter to the US, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 10, 2011K102508YU LONG SHENG DISPOSABLE THERMOMETER SHEATHS, MODELS YLS-01 AND YLS-02FLLSubstantially EquivalentYu Long Sheng Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated January 10, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.