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Data / Medical devices / China / Zhejiang Gongdong Medical Technology Co., Ltd

Zhejiang Gongdong Medical Technology Co., Ltd: FDA-registered device maker in TAIZHOU Zhejiang, China, 5 510(k) clearances

Zhejiang Gongdong Medical Technology Co., Ltd is registered with the FDA (registration 3005739529) in TAIZHOU Zhejiang, China. It lists 39 device types. The FDA files 5 510(k) clearances under its listings, the newest dated December 22, 2025. Registered through 2027. FDA data exported November 3, 2026.

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Get makers like this oneWatch Zhejiang Gongdong Medical Technology Co., Ltd
FDA registration number
3005739529
Address
a)No 10 & 39,Beiyuan Ave. b)No.88 Jingxian Rd. Huangyan, TAIZHOU Zhejiang, China, 318020
Owner or operator
ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD. (9072045)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
May 15, 2006
Registered through
2027
Brand names listed
20ml Dosage cup, A SPECIFIC MEDICAL USE, APPLICATOR, ABSORBENT TIPPED sterile, sampling swab kit Sterile,, Absorbent tipped applicator; Sampling Swab, Biohazard Bags, Biopsy foam pads;embedding rings;storage drawer;tissue capsules, CONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE, Capilary Blood Collection Tubes 9NC Coagulation Sodium Citrate 3.2%; and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Contract manufacturer, Manufactureraccessdata.fda.gov
Applicator, Absorbent Tipped, Non-SterileKXF1Manufactureraccessdata.fda.gov
Applicator, Absorbent Tipped, SterileKXG1Manufactureraccessdata.fda.gov
Basin, EmesisFNY1Manufactureraccessdata.fda.gov
Blood Specimen Collection Convenience Kit (Excludes Hiv)PQD2Manufactureraccessdata.fda.gov
Bottle, Collection, VacuumKDQ2Manufactureraccessdata.fda.gov
Bottle, Roller, Tissue CultureKJC1Manufactureraccessdata.fda.gov
Cassettes, TissueIDZ1Manufactureraccessdata.fda.gov
Container, SharpsMMK2Manufactureraccessdata.fda.gov
Container, Specimen Mailer And Storage, Non-SterileNNK1Manufactureraccessdata.fda.gov
Container, Specimen Mailer And Storage, Temperature Controlled, Non-SterileNNL1Manufactureraccessdata.fda.gov
Container, Specimen, Non-SterileNNI1Manufactureraccessdata.fda.gov
Container, Specimen, SterileFMH1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Culture Media, Non-Propagating TransportJSM1Manufactureraccessdata.fda.gov
Culture Media, Non-Selective And Non-DifferentialJSG1Manufactureraccessdata.fda.gov
Curette, EarJYG1Contract manufacturer, Manufactureraccessdata.fda.gov
Cuvette, ThermostatedJRI1Manufactureraccessdata.fda.gov
Depressor, Tongue, Non-SurgicalFMA1Manufactureraccessdata.fda.gov
Device, Specimen CollectionLIO1Manufactureraccessdata.fda.gov
Dish, Tissue CultureKIZ1Manufactureraccessdata.fda.gov
Dispenser, Liquid MedicationKYX1Manufactureraccessdata.fda.gov
Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical UseLXG1Manufactureraccessdata.fda.gov
ForcepsHTD1Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Manufactureraccessdata.fda.gov
Light, Surgical, AccessoriesFTA2Contract manufacturer, Manufactureraccessdata.fda.gov
Micro PipetteJRC1Manufactureraccessdata.fda.gov
OtoscopeERA1Manufactureraccessdata.fda.gov
Pack, Hot Or Cold, DisposableIMD1Manufactureraccessdata.fda.gov
Pad, Alcohol, Device DisinfectantLKBUManufactureraccessdata.fda.gov
Retractor, VaginalHDL1Manufactureraccessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)HOY1Contract manufactureraccessdata.fda.gov
Speculum, EntEPY1Manufactureraccessdata.fda.gov
Speculum, RectalFFQ1Manufactureraccessdata.fda.gov
Speculum, Vaginal, NonmetalHIB2Manufactureraccessdata.fda.gov
Tourniquet, NonpneumaticGAX1Manufactureraccessdata.fda.gov
Trap, Sterile SpecimenBYZ2Manufactureraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Manufactureraccessdata.fda.gov
Tube, Collection, Capillary BloodGIO1Manufactureraccessdata.fda.gov
Urine Collection Kit (Excludes Hiv Testing)OIE1Contract manufacturer, 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
December 22, 2025K253222Gongdong Sharps Container (SCR-01Q, SCR-01G, SCR-03G)MMKSubstantially EquivalentZhejiang Gongdong Medical Technology Co., Ltd.accessdata.fda.gov
November 17, 2022K220739Disposable Urine Collection TubeJSMSubstantially EquivalentZhejiang Gongdong Medical Technology Co., Ltd.accessdata.fda.gov
November 12, 2020K201523Sharps containerMMKSubstantially EquivalentZhejiang Gongdong Medical Technology Co., Ltd.accessdata.fda.gov
September 3, 2008K082042GONGDONG DISPOSABLE SHARP CONTAINERMMKSubstantially EquivalentZhejiang Gongdong Medical Plastic Factoryaccessdata.fda.gov
July 11, 2005K050887GONGDONG DISPOSABLE VAGINAL SPECULUMHIBSubstantially EquivalentZhejiang Gongdong Medical Plastic Factoryaccessdata.fda.gov

Compare with other makers

Updated December 22, 2025. 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.