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Data / Medical devices / Solution, Decalcifier, Acid Containing / United States

FDA-registered makers of Solution, Decalcifier, Acid Containing in the United States: 13 establishments

13 establishments in the United States are registered with the FDA to make Solution, Decalcifier, Acid Containing (product code KDX). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Solution, Decalcifier, Acid Containing
Product code
KDX
Country
United States

Makers of Solution, Decalcifier, Acid Containing in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Azer Scientific, Inc.Morgantown, PA, United StatesComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
Cancer Diagnostics, Inc.Durham, NC, United StatesManufacturer0000api.fda.gov
E K Industries, Inc.Joliet, IL, 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
Medical Chemical CorporationTorrance, CA, United StatesManufacturer0000api.fda.gov
Newcomer Supply IncWaunakee, WI, United StatesSpecification developer0000api.fda.gov
Reprocessing Products Corporation (RPC)Tucson, AZ, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Ricca Chemical Company LLCPocomoke City, MD, United StatesManufacturer0000api.fda.gov
Ricca Chemical Company LLCArlington, TX, United StatesManufacturer0000api.fda.gov
Ricca Chemical Company LLCBatesville, IN, United StatesManufacturer0000api.fda.gov
Richard-Allan Scientific LLCKalamazoo, MI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
SLMP LLC d.b.a. StatLab Medical ProductsMcKinney, TX, 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.