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

FDA-registered makers of Culture Media, Non-Selective And Differential in the United States: 15 establishments

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

15 establishments in the United States are registered with the FDA to make Culture Media, Non-Selective And Differential (product code JSH). 1 has a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device: Culture Media, Non-Selective And Differential
Product code: JSH
Country: United States

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

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Hardy Diagnostics	Orcutt, CA, United States	Manufacturer	2	March 31, 1988	0	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
Becton, Dickinson & Co.	Sparks, MD, United States	Complaint file establishment, Specification developer	0		0	api.fda.gov
Becton, Dickinson & Co.	Cockeysville, MD, United States	Manufacturer	0		0	api.fda.gov
Hardy Diagnostics	Springboro, OH, United States	Manufacturer	0		0	api.fda.gov
Inter-Med, Inc.	Racine, WI, United States	Manufacturer	0		0	api.fda.gov
K&R Technologies Dba Microbiology International	Frederick, MD, United States	Manufacturer	0		0	api.fda.gov
Legacy Biologicals	Baltimore, MD, United States	Manufacturer	0		0	api.fda.gov
Lifesign L.L.C.	Skillman, NJ, United States	Manufacturer	0		0	api.fda.gov
Neogen Culture Media	Lansing, MI, United States	Manufacturer	0		0	api.fda.gov
Remel, Inc.	Lenexa, KS, United States	Manufacturer	0		2	api.fda.gov
S2media	Spokane Valley, WA, United States	Manufacturer	0		0	api.fda.gov
Teresita Biolab LLC	Bayamon, PR, United States	Manufacturer	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.