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Data / Medical devices / United States / Chembio Diagnostic Systems

Chembio Diagnostic Systems: FDA-registered device maker in Bay Shore, NY, United States, 4 510(k) clearances

Chembio Diagnostic Systems is registered with the FDA (registration 3026565854) in Bay Shore, NY, United States. It lists 18 device types. The FDA files 4 510(k) clearances under its listings, the newest dated September 29, 2023. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3026565854
Address
1560 Fifth Avenue, Bay Shore, NY, United States, 11706
Owner or operator
CHEMBIO DIAGNOSTIC SYSTEMS, INC. (2431980)
Roles
Complaint file establishment, Manufacturer for export
First device listed
December 3, 2007
Registered through
2027
Brand names listed
Adalimumab Assay, C-Reactive Protein, Antigen, Antiserum and Control, Chembio HIV 1/2 STAT PAK Assay, DPP Ebola Antigen System, DPP HIV, DPP HIV 1/2 Assay, DPP HIV-Syphilis, DPP Zika IgM System, DPP Zika IgM System Control Pack, and DPP Micro Reader and more

Devices it lists

DeviceProduct codeClassRoleSource
Adalimumab AssayQYD2Complaint file establishmentaccessdata.fda.gov
Antigens, Nontreponemal, AllGMQ2Manufacturer for exportaccessdata.fda.gov
Assayed Quality Control Material For Clinical Microbiology AssaysQCH2Complaint file establishmentaccessdata.fda.gov
C-Reactive Protein, Antigen, Antiserum, And ControlDCK2Complaint file establishmentaccessdata.fda.gov
Colorimeter, Photometer, Spectrophotometer For Clinical UseJJQ1Complaint file establishmentaccessdata.fda.gov
Coronavirus Antigen Detection Test System.QKPNManufacturer for exportaccessdata.fda.gov
Dengue Serological ReagentsOSU2Manufacturer for exportaccessdata.fda.gov
Devices Detecting Influenza A, B, And C Virus AntigensPSZ2Manufacturer for exportaccessdata.fda.gov
Enzyme Linked Immunoabsorption Assay, Treponema PallidumLIP2Manufacturer for exportaccessdata.fda.gov
Enzyme Linked Immunosorbent Assay, T. CruziMIU1Manufacturer for exportaccessdata.fda.gov
Infliximab Test SystemQXT2Complaint file establishmentaccessdata.fda.gov
Kit, Test, Saliva, Hiv-1&2MWB3Manufacturer for exportaccessdata.fda.gov
Reagent, Coronavirus SerologicalQKONManufacturer for exportaccessdata.fda.gov
Reagents, Ebola Zaire Virus (Detected In The West Africa Outbreak In 2014) Nucleic AcidPOGNManufacturer for exportaccessdata.fda.gov
System, Nucleic Acid Amplification, Mycobacterium Tuberculosis ComplexMWA2Manufacturer for exportaccessdata.fda.gov
Test, Hiv DetectionMZF2Complaint file establishment, Manufacturer for exportaccessdata.fda.gov
Test, Qualitative, Detection Of Dengue Igm And Igg AntibodiesNWYNManufacturer for exportaccessdata.fda.gov
Zika Virus Serological ReagentsQFO2Complaint file establishmentaccessdata.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
September 29, 2023DEN220023Procise ADLQYDUnknownProcisedx, Inc.accessdata.fda.gov
September 29, 2023DEN210056Procise IFXQXTUnknownProcisedx, Inc.accessdata.fda.gov
November 4, 2022K201256Procise CRP, ProciseDx Analyzer, ProciseDx Calibration CartridgeDCKSubstantially EquivalentProcise Diagnosticsaccessdata.fda.gov
June 3, 2020K200506DPP Zika IgM System, DPP Zika IgM System Control Pack, and DPP Micro ReaderQFOSubstantially EquivalentChembio Diagnostic Systemsaccessdata.fda.gov

Compare with other makers

Updated September 29, 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.