Data / Medical devices / Culture Media, General Nutrient Broth
Culture Media, General Nutrient Broth (JSC): 15 FDA-registered makers in 5 countries
15 establishments in 5 countries are registered with the FDA to make Culture Media, General Nutrient Broth (product code JSC, Class 1, 21 CFR 866.2350). 2 of them have a 510(k) clearance or PMA approval on file and 3 have a recall event. The FDA has issued 52 510(k) clearances under this code, the latest on March 5, 1985, and lists 5 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- JSC
- Device class
- 1
- Regulation
- 866.2350
- Medical specialty
- Microbiology
Makers by country
| Country | Makers |
|---|---|
| United States | 9 |
| France | 2 |
| India | 2 |
| United Kingdom | 1 |
| China | 1 |
Makers of Culture Media, General Nutrient 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 | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Oxoid, Ltd. | Basingstoke, Hampshire, United Kingdom | Exporter to the US, Manufacturer | 1 | September 21, 1982 | 0 | 0 | 0 | api.fda.gov |
| Remel, Inc. | Lenexa, KS, United States | Manufacturer | 1 | May 3, 1979 | 0 | 1 | 0 | api.fda.gov |
| Anaerobe Systems | Morgan Hill, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Analytichem Usa, Inc. | Winslow, ME, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Becton, Dickinson & Co. | Sparks, MD, United States | Complaint file establishment, Specification developer | 0 | 0 | 2 | 0 | api.fda.gov | |
| Becton, Dickinson & Co. | Cockeysville, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomerieux SA | LA BALME LES GROTTES Isere, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chromagar | Saint-Denis Seine-Saint-Denis, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hardy Diagnostics | Orcutt, CA, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Himedia Laboratories Private Limited | DOMBIVLI, THANE Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Himedia Laboratories Private Limited | NASHIK Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hardy Diagnostics | Springboro, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiaoyue Pharmaceutical (huizhou) Co.ltd | Huizhou Guangdong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Key Scientific Products | Stamford, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Legacy Biologicals | Baltimore, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 5, 1985. 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.