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Data / Medical devices / Culture Media, Non-Propagating Transport / United States

FDA-registered makers of Culture Media, Non-Propagating Transport in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Culture Media, Non-Propagating Transport (product code JSM). 14 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Culture Media, Non-Propagating Transport
Product code
JSM
Country
United States

Makers of Culture Media, Non-Propagating Transport in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Remel, Inc.Lenexa, KS, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler5September 18, 1996010api.fda.gov
Copan Diagnostics, Inc.Murrieta, CA, United StatesContract manufacturer, Repackager or relabeler2April 10, 2015000api.fda.gov
Medical Chemical CorporationTorrance, CA, United StatesManufacturer2May 29, 2015000api.fda.gov
Meridian Bioscience, Inc.Cincinnati, OH, United StatesManufacturer2August 28, 1985000api.fda.gov
Medegen Medical ProductsGallaway, TN, United StatesSpecification developer2August 13, 2003000api.fda.gov
Puritan Medical Products Company LLCGuilford, ME, United StatesManufacturer2November 4, 2016000api.fda.gov
Trinity Biotech USAJamestown, NY, United StatesManufacturer2August 15, 1994000api.fda.gov
Aceso Laboratories Inc.Chino, CA, United StatesManufacturer1April 4, 2025000api.fda.gov
Arx SciencesAmherst, NY, United StatesManufacturer1March 19, 2024000api.fda.gov
Becton DickinsonFranklin Lakes, NJ, United StatesSpecification developer1March 26, 2003010api.fda.gov
Becton, Dickinson & Co.Broken Bow, NE, United StatesManufacturer1March 26, 2003000api.fda.gov
COPAN Diagnostics, Inc.Carlsbad, CA, United StatesContract manufacturer, Repackager or relabeler1December 7, 2004000api.fda.gov
Hardy DiagnosticsOrcutt, CA, United StatesManufacturer1August 2, 2024010api.fda.gov
Hardy DiagnosticsSpringboro, OH, United StatesManufacturer1August 2, 2024000api.fda.gov
Azer Scientific, Inc.Morgantown, PA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
CepheidSunnyvale, CA, United StatesManufacturer, Specification developer0010api.fda.gov
CepheidLodi, CA, United StatesManufacturer0000api.fda.gov
Copan Industries, Inc.Aguadilla, PR, United StatesContract manufacturer0000api.fda.gov
Immco Diagnostics, Inc.Williamsville, NY, United StatesContract manufacturer0000api.fda.gov
MML Diagnostics Packaging, Inc.Troutdale, OR, United StatesContract manufacturer0000api.fda.gov
STS CorporationDuluth, GA, United StatesComplaint file establishment, Repackager or relabeler, Specification 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.