Data / Medical devices / Culture Media, Non-Selective And Non-Differential / United States

FDA-registered makers of Culture Media, Non-Selective And Non-Differential in the United States: 24 establishments

Name: FDA-registered makers of Culture Media, Non-Selective And Non-Differential in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

24 establishments in the United States are registered with the FDA to make Culture Media, Non-Selective And Non-Differential (product code JSG). 1 has 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, Non-Selective And Non-Differential
Product code: JSG
Country: United States

Makers of Culture Media, Non-Selective And Non-Differential in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Remel, Inc.	Lenexa, KS, United States	Manufacturer, Specification developer	1	October 31, 1980	4	api.fda.gov
Alpha Biosciences, Inc.	Baltimore, MD, United States	Manufacturer, Remanufacturer, Repackager or relabeler	0		0	api.fda.gov
Anaerobe Systems	Morgan Hill, CA, United States	Complaint file establishment, Manufacturer	0		0	api.fda.gov
Analytichem Usa, Inc.	Winslow, ME, United States	Manufacturer	0		0	api.fda.gov
Arx Sciences	Amherst, NY, United States	Manufacturer	0		0	api.fda.gov
Becton, Dickinson & Co.	Sparks, MD, United States	Complaint file establishment, Specification developer	0		4	api.fda.gov
Becton, Dickinson & Co.	Cockeysville, MD, United States	Manufacturer	0		0	api.fda.gov
Biomerieux, Inc.	Lombard, IL, United States	Contract manufacturer	0		0	api.fda.gov
Beckman Coulter, Inc.	West Sacramento, CA, United States	Manufacturer	0		0	api.fda.gov
Becton, Dickinson and Company	Mebane, NC, United States	Manufacturer	0		0	api.fda.gov
Copan Diagnostics, Inc.	Murrieta, CA, United States	Manufacturer	0		0	api.fda.gov
Deroyal Industries, Inc.	Powell, TN, United States	Complaint file establishment, Specification developer	0		0	api.fda.gov
Diagnostic Consulting Network, LLC.	Carlsbad, CA, United States	Manufacturer	0		0	api.fda.gov
Hardy Diagnostics	Orcutt, CA, United States	Manufacturer	0		0	api.fda.gov
Hardy Diagnostics	Springboro, OH, United States	Manufacturer	0		0	api.fda.gov
Key Scientific Products	Stamford, TX, United States	Manufacturer	0		0	api.fda.gov
Labone, Inc.	Lenexa, KS, United States	Specification developer	0		0	api.fda.gov
Legacy Biologicals	Baltimore, MD, United States	Manufacturer	0		0	api.fda.gov
Oxyrase, Inc.	Mansfield, OH, United States	Manufacturer	0		0	api.fda.gov
Puritan Medical Products Company LLC	Guilford, ME, United States	Manufacturer	0		0	api.fda.gov
Precision Medical Devices Inc	New Brunswick, NJ, United States	Repackager or relabeler, Specification developer	0		0	api.fda.gov
S2media	Spokane Valley, WA, United States	Manufacturer	0		0	api.fda.gov
Trademark Plastics Inc.	Riverside, CA, United States	Specification developer	0		0	api.fda.gov
Xcaliber Sciences, Inc.	San Diego, CA, United States	Specification developer	0		0	api.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.