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Data / Medical devices / Slides, Microscope / United States

FDA-registered makers of Slides, Microscope in the United States: 28 establishments

28 establishments in the United States are registered with the FDA to make Slides, Microscope (product code KEW). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Slides, Microscope
Product code
KEW
Country
United States

Makers of Slides, Microscope in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abbott LaboratoriesIrving, TX, United StatesSpecification developer0000api.fda.gov
ANATECH division of Cancer Diagnostics, Inc.Battle Creek, MI, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Azer Scientific, Inc.Morgantown, PA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Alltrista Plastics LLCReedsville, PA, United StatesManufacturer0000api.fda.gov
Becton, Dickinson & Co.Sparks, MD, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Bio SB, Inc.Santa Barbara, CA, United StatesSpecification developer0000api.fda.gov
Biogenex Laboratories Inc.Fremont, CA, United StatesManufacturer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Becton, Dickinson and CompanyMebane, NC, United StatesManufacturer0000api.fda.gov
Biomedical Polymers, Inc.Sterling, MA, United StatesManufacturer0000api.fda.gov
Cell Marque Corp.Saint Louis, MO, United StatesManufacturer0000api.fda.gov
Cell Marque Corp.Rocklin, CA, United StatesManufacturer0000api.fda.gov
CalibreScientific US, Inc.Vancouver, WA, United StatesManufacturer0000api.fda.gov
Caplugs, Inc.Rancho Dominguez, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Hardy DiagnosticsOrcutt, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Hologic, Inc.Marlborough, MA, United StatesSpecification developer0010api.fda.gov
IMMY, Inc.Norman, OK, United StatesSpecification developer0000api.fda.gov
Kova International IncGarden Grove, CA, United StatesManufacturer0000api.fda.gov
Leica Biosystems Richmond, Inc.Richmond, IL, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
New Erie Scientific LLCPortsmouth, NH, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Sakura Finetek U.s.a., Inc.Torrance, CA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
SLMP LLC d.b.a. StatLab Medical ProductsArlington, TX, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Springside Scientific LLCDurham, NC, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Ventana Medical Systems, Inc.Tucson, AZ, United StatesManufacturer0000api.fda.gov
VolusolTooele, UT, United StatesManufacturer0000api.fda.gov
Welmed, Inc.Chicago, IL, United StatesSpecification developer0000api.fda.gov

Updated November 2, 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.