Data / Medical devices / Culture Media, Selective Broth

Culture Media, Selective Broth (JSD): 18 FDA-registered makers in 8 countries

Name: FDA-registered makers of Culture Media, Selective Broth
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

18 establishments in 8 countries are registered with the FDA to make Culture Media, Selective Broth (product code JSD, Class 1, 21 CFR 866.2360). 3 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 26 510(k) clearances under this code, the latest on August 15, 1988, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code: JSD
Device class: 1
Regulation: 866.2360
Medical specialty: Microbiology

Makers by country

Country	Makers
United States	9
France	2
India	2
Spain	1
Italy	1
Taiwan	1
Belgium	1
United Kingdom	1

Makers of Culture Media, Selective Broth

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Becton, Dickinson & Co.	Sparks, MD, United States	Complaint file establishment, Specification developer	1	December 16, 1983	1	api.fda.gov
Becton, Dickinson & Co.	Cockeysville, MD, United States	Manufacturer	1	December 16, 1983	0	api.fda.gov
Remel, Inc.	Lenexa, KS, United States	Manufacturer	1	May 13, 1987	1	api.fda.gov
Analytichem Usa, Inc.	Winslow, ME, United States	Manufacturer	0		0	api.fda.gov
Biomerieux France	CRAPONNE Rhone, France	Manufacturer	0		0	api.fda.gov
Biomerieux Spain	Tres Cantos Madrid(Province), Spain	Manufacturer	0		0	api.fda.gov
Chromagar	Saint-Denis Seine-Saint-Denis, France	Manufacturer	0		0	api.fda.gov
Copan Diagnostics, Inc.	Murrieta, CA, United States	Manufacturer	0		0	api.fda.gov
Copan Italia	BRESCIA Lombardy, Italy	Manufacturer	0		0	api.fda.gov
Creative Life Science Co., Ltd.	Xinzhuang District New Taipei, Taiwan	Manufacturer	0		0	api.fda.gov
Hardy Diagnostics	Orcutt, CA, United States	Manufacturer	0		0	api.fda.gov
Himedia Laboratories Private Limited	DOMBIVLI, THANE Maharashtra, India	Manufacturer	0		0	api.fda.gov
Himedia Laboratories Private Limited	NASHIK Maharashtra, India	Manufacturer	0		0	api.fda.gov
Hardy Diagnostics	Springboro, OH, United States	Manufacturer	0		0	api.fda.gov
Legacy Biologicals	Baltimore, MD, United States	Manufacturer	0		0	api.fda.gov
Lonza Walkersville, Inc.	Walkersville, MD, United States	Contract manufacturer, Manufacturer	0		0	api.fda.gov
Lonza Verviers SRL.	Verviers Liege, Belgium	Contract manufacturer	0		0	api.fda.gov
Oxoid, Ltd.	Basingstoke, Hampshire, United Kingdom	Exporter to the US, Manufacturer	0		0	api.fda.gov

Updated August 15, 1988. 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.