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Data / Medical devices / Enzyme Immunoassay, Propoxyphene / United States

FDA-registered makers of Enzyme Immunoassay, Propoxyphene in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Enzyme Immunoassay, Propoxyphene (product code JXN). 12 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Enzyme Immunoassay, Propoxyphene
Product code
JXN
Country
United States

Makers of Enzyme Immunoassay, Propoxyphene in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Microgenics CorporationFremont, CA, United StatesContract manufacturer, Manufacturer2May 2, 1995000api.fda.gov
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesManufacturer2May 10, 2001000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer2February 1, 2000000api.fda.gov
Alfa Scientific Designs, Inc.Poway, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler1November 29, 2002000api.fda.gov
Alere San Diego, Inc.San Diego, CA, United StatesSpecification developer1May 19, 2004000api.fda.gov
Beckman Coulter, Inc.Brea, CA, United StatesSpecification developer1February 9, 1996000api.fda.gov
Bio-Rad Laboratories, Inc.Hercules, CA, United StatesSpecification developer1May 19, 2004000api.fda.gov
Germaine Laboratories, Inc.San Antonio, TX, United StatesManufacturer, Repackager or relabeler1May 19, 2004000api.fda.gov
Lin-Zhi International, Inc.Santa Clara, CA, United StatesManufacturer1January 21, 2003000api.fda.gov
Medica Corp.Bedford, MA, United StatesManufacturer1December 6, 2011000api.fda.gov
Medtox Diagnostics, Inc.Burlington, NC, United StatesManufacturer1May 2, 2002000api.fda.gov
Medtox Diagnostics, Inc.Burlington, NC, United StatesManufacturer1May 2, 2002000api.fda.gov
Advin Biotech, Inc.San Diego, CA, United StatesManufacturer0000api.fda.gov
Beckman Coulter, Inc.Carlsbad, CA, United StatesContract manufacturer0000api.fda.gov
Calbiotech, Inc.El Cajon, CA, United StatesManufacturer for export, Repackager or relabeler0000api.fda.gov
Chemtron Biotech, Inc.San Diego, CA, United StatesComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
Healgen Scientific LLCHouston, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Medical Disposables CorpOrlando, FL, United StatesComplaint file establishment, Manufacturer for export, Repackager or relabeler0000api.fda.gov
Ucp Biosciences, Inc.Milpitas, CA, United StatesSpecification developer0000api.fda.gov

Updated November 3, 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.