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
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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 29, 2023 | DEN220023 | Procise ADL | QYD | Unknown | Procisedx, Inc. | accessdata.fda.gov |
| September 29, 2023 | DEN210056 | Procise IFX | QXT | Unknown | Procisedx, Inc. | accessdata.fda.gov |
| November 4, 2022 | K201256 | Procise CRP, ProciseDx Analyzer, ProciseDx Calibration Cartridge | DCK | Substantially Equivalent | Procise Diagnostics | accessdata.fda.gov |
| June 3, 2020 | K200506 | DPP Zika IgM System, DPP Zika IgM System Control Pack, and DPP Micro Reader | QFO | Substantially Equivalent | Chembio Diagnostic Systems | accessdata.fda.gov |
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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.