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Data / Medical devices / China / Guangdong Bingbing Health Care Products Ltd.

Guangdong Bingbing Health Care Products Ltd.: FDA-registered device maker in Jiangmen Guangdong, China, 6 510(k) clearances

Guangdong Bingbing Health Care Products Ltd. is registered with the FDA (registration 3017654286) in Jiangmen Guangdong, China. It lists 7 device types. The FDA files 6 510(k) clearances under its listings, the newest dated December 15, 2023. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3017654286
Address
No. 71, Xinyue 3rd Road, Liyue Street, Jianghai District, Jiangmen Guangdong, China, 529000
Owner or operator
Guangdong Bingbing Health Care Products Ltd. (10078439)
Roles
Exporter to the US, Manufacturer, Repackager or relabeler
First device listed
October 22, 2020
Registered through
2026
Brand names listed
Absorbent Sweat Pad, Adult Diapers, Disposable Face Masks, Incontinence Pad, Maternity Pad, Panty Liner, Protective Underwear, Sanitary Napkin and more

Devices it lists

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
December 15, 2023K232598Unscented Menstrual TamponHEBSubstantially EquivalentUnibeauty (Hubei) Technology Co., Ltd.accessdata.fda.gov
December 20, 2019K191666Unscented W long plastic and cardboard applicator tamponsHEBSubstantially EquivalentOntex Bvbaaccessdata.fda.gov
March 3, 2017K162746Ontex and other proprietary namesHEBSubstantially EquivalentOntex Bvbaaccessdata.fda.gov
July 2, 2015K151170Tosama 100% Organic Cotton Menstrual TamponHEBSubstantially EquivalentTosama, D.O.O.accessdata.fda.gov
December 23, 2009K090819ONTEX TAMPON (UNSCENTED)HEBSubstantially EquivalentOntex International NVaccessdata.fda.gov
September 10, 2008K080775MAXIM PLASTIC APPLICATOR & NON-APPLICATOR TAMPONSHEBSubstantially EquivalentTosama D.D.accessdata.fda.gov

Compare with other makers

Updated December 15, 2023. 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.