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Data / Medical devices / China / Ningbo Sincerecare Import And Export Co.,ltd

Ningbo Sincerecare Import And Export Co.,ltd: FDA-registered device maker in NINGBO Zhejiang, China, 1 510(k) clearance

Ningbo Sincerecare Import And Export Co.,ltd is registered with the FDA (registration 3011611571) in NINGBO Zhejiang, China. It lists 16 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 22, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3011611571
Address
#502, No.43 Cangsong Road, NINGBO Zhejiang, China, 315012
Owner or operator
NINGBO SINCERECARE IMPORT AND EXPORT CO.,LTD (10049212)
Roles
Exporter to the US
First device listed
April 29, 2015
Registered through
2026
Brand names listed
ALCOHOL PREP PAD,BZK TOWELETTE, ARM SLING,TRIANGULAR BANDAGE, CALIPERS AND RULERS,TAPE MEASURING, DISPOSAL BAG,VOMIT BAG, GAUZE PAD,GAUZE ROLL,GAUZE COMPRESS,GAUZE BANDAGE, Otoscope, PENLIGHT, REFLEX HAMMER,NEURO HAMMER and more

Devices it lists

DeviceProduct codeClassRoleSource
Aid, TransferIKX1Exporter to the USaccessdata.fda.gov
Basin, EmesisFNY1Exporter to the USaccessdata.fda.gov
Container, SharpsMMK2Exporter to the USaccessdata.fda.gov
Container, Specimen, Non-SterileNNI1Exporter to the USaccessdata.fda.gov
Disinfectant, Medical DevicesLRJ1Exporter to the USaccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Exporter to the USaccessdata.fda.gov
Light, Examination, Medical, Battery PoweredKYT1Exporter to the USaccessdata.fda.gov
OtoscopeERA1Exporter to the USaccessdata.fda.gov
PercussorGWZ1Exporter to the USaccessdata.fda.gov
Sling, Arm, Overhead SupportedILE1Exporter to the USaccessdata.fda.gov
Splint, Hand, And ComponentsILH1Exporter to the USaccessdata.fda.gov
Stethoscope, ManualLDE1Exporter to the USaccessdata.fda.gov
Stretcher, Hand-CarriedFPP1Exporter to the USaccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Exporter to the USaccessdata.fda.gov
Tape, Measuring, Rulers And CalipersFTY1Exporter to the USaccessdata.fda.gov
Tourniquet, NonpneumaticGAX1Exporter to the USaccessdata.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
May 22, 2026K253773Guanhong Sharps Container (GHW-1F1); Guanhong Sharps Container (GHW-1F4); Guanhong Sharps Container (GH-6FA); Guanhong Sharps Container (GHW-2FR); Guanhong Sharps Container (GHW-8FR); Guanhong Sharps Container (GH-3FS); Guanhong Sharps Container (GHW-15FS); Guanhong Sharps Container (GHW-27FS); Guanhong Sharps Container (GH-5FSW); Guanhong Sharps Container (GHW-3FT); Guanhong Sharps Container (GHW-4FT); Guanhong Sharps Container (GHW-5FT); Guanhong Sharps Container (GHW-8FT); GuanhongMMKSubstantially EquivalentTaizhou Huangyan Guanhong Plastic Steel Products Factoryaccessdata.fda.gov

Compare with other makers

Updated May 22, 2026. 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.