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Data / Medical devices / Culture Media, For Isolation Of Pathogenic Neisseria / United States

FDA-registered makers of Culture Media, For Isolation Of Pathogenic Neisseria in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Culture Media, For Isolation Of Pathogenic Neisseria (product code JTY). 6 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.

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Device
Culture Media, For Isolation Of Pathogenic Neisseria
Product code
JTY
Country
United States

Makers of Culture Media, For Isolation Of Pathogenic Neisseria in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Hardy DiagnosticsOrcutt, CA, United StatesManufacturer3December 17, 1993000api.fda.gov
Becton, Dickinson & Co.Sparks, MD, United StatesComplaint file establishment, Specification developer1October 7, 1976060api.fda.gov
Becton, Dickinson & Co.Cockeysville, MD, United StatesManufacturer1October 7, 1976000api.fda.gov
Diagnostic Consulting Network, LLC.Carlsbad, CA, United StatesManufacturer1December 16, 1999000api.fda.gov
Hardy DiagnosticsSpringboro, OH, United StatesManufacturer1July 6, 1982000api.fda.gov
Remel, Inc.Lenexa, KS, United StatesManufacturer1February 16, 1996020api.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.