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Data / Medical devices / Fixative, Formalin-Containing / United States

FDA-registered makers of Fixative, Formalin-Containing in the United States: 14 establishments

14 establishments in the United States are registered with the FDA to make Fixative, Formalin-Containing (product code LDY). 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
Fixative, Formalin-Containing
Product code
LDY
Country
United States

Makers of Fixative, Formalin-Containing in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Azer Scientific, Inc.Morgantown, PA, United StatesComplaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Cancer Diagnostics, Inc.Durham, NC, United StatesManufacturer0000api.fda.gov
Delasco, LLCPlano, TX, United StatesManufacturer0000api.fda.gov
Ethos Biosciences, INC.Logan Township, NJ, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Leica Biosystems Richmond, Inc.Richmond, IL, United StatesManufacturer0000api.fda.gov
Life Technologies CorporationFrederick, MD, United StatesManufacturer0000api.fda.gov
Medical Chemical CorporationTorrance, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Michclone Associates, Inc.Troy, MI, United StatesManufacturer0000api.fda.gov
Newcomer Supply IncWaunakee, WI, United StatesSpecification developer0000api.fda.gov
Richard-Allan Scientific LLCKalamazoo, MI, United StatesManufacturer0011api.fda.gov
Scytek Laboratories, Inc.Logan, UT, United StatesManufacturer0000api.fda.gov
SLMP LLC d.b.a. StatLab Medical ProductsMcKinney, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
SSN SolutionsHenrico, VA, United StatesManufacturer0000api.fda.gov
VolusolTooele, UT, United StatesManufacturer0000api.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.