Data / Medical devices / Culture Media, Selective And Differential / United States
FDA-registered makers of Culture Media, Selective And Differential in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Culture Media, Selective And Differential (product code JSI). 3 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 3, 2026.
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- Device
- Culture Media, Selective And Differential
- Product code
- JSI
- Country
- United States
Makers of Culture Media, Selective And Differential in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Remel, Inc. | Lenexa, KS, United States | Manufacturer | 7 | June 24, 1987 | 0 | 4 | 0 | api.fda.gov |
| Becton, Dickinson & Co. | Sparks, MD, United States | Complaint file establishment, Specification developer | 1 | November 20, 2007 | 0 | 5 | 0 | api.fda.gov |
| Becton, Dickinson & Co. | Cockeysville, MD, United States | Manufacturer | 1 | November 20, 2007 | 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 | 1 | 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 | |
| Hardy Diagnostics | Springboro, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| K&R Technologies Dba Microbiology International | Frederick, MD, United States | 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 | |
| Lifesign L.L.C. | Skillman, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| S2media | Spokane Valley, WA, United States | Manufacturer | 0 | 0 | 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.