Data / Medical devices / Culture Media, Selective And Non-Differential
Culture Media, Selective And Non-Differential (JSJ): 24 FDA-registered makers in 7 countries
24 establishments in 7 countries are registered with the FDA to make Culture Media, Selective And Non-Differential (product code JSJ, Class 1, 21 CFR 866.2360). 2 of them have a 510(k) clearance or PMA approval on file and 3 have a recall event. The FDA has issued 307 510(k) clearances under this code, the latest on June 22, 1988, and lists 4 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- JSJ
- Device class
- 1
- Regulation
- 866.2360
- Medical specialty
- Microbiology
Makers by country
| Country | Makers |
|---|---|
| United States | 15 |
| India | 3 |
| United Kingdom | 2 |
| Italy | 1 |
| Taiwan | 1 |
| China | 1 |
| South Korea | 1 |
Makers of Culture Media, Selective And Non-Differential
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 |
|---|---|---|---|---|---|---|---|---|
| Remel, Inc. | Lenexa, KS, United States | Manufacturer | 5 | January 11, 1984 | 0 | 1 | 0 | api.fda.gov |
| Oxoid, Ltd. | Basingstoke, Hampshire, United Kingdom | Exporter to the US, Manufacturer | 4 | May 11, 1984 | 0 | 0 | 0 | api.fda.gov |
| Alpha Biosciences, Inc. | Baltimore, MD, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 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 | 1 | 0 | api.fda.gov | |
| Becton, Dickinson & Co. | Cockeysville, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Copan Italia | BRESCIA Lombardy, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Creative Life Science Co., Ltd. | Xinzhuang District New Taipei, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CalibreScientific US, Inc. | Vancouver, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diagnostic Consulting Network, LLC. | Carlsbad, CA, United States | 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 | |
| Himedia Laboratories Private Limited | Thane Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hardy Diagnostics | Springboro, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jinan Babio Biotechnology Co.,ltd. | Jinan City Shandong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Legacy Biologicals | Baltimore, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Wire And Equipment Co. Ltd. | Corsham, Wiltshire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oxyrase, Inc. | Mansfield, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Puritan Medical Products Company LLC | Guilford, ME, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quality Bioresources, Inc | Seguin, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| S2media | Spokane Valley, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yong Chang Co., Ltd. | Gimpo Gyeonggi, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 22, 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.